{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,9]],"date-time":"2026-11-09T23:30:36Z","timestamp":1794267036881,"version":"4.9.0"},"reference-count":101,"publisher":"Springer Science and Business Media LLC","issue":"1","content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Orphanet J Rare Dis"],"published-print":{"date-parts":[[2006,12]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    The Cri du Chat syndrome (CdCS) is a genetic disease resulting from a deletion of variable size occurring on the short arm of chromosome 5 (5p-). The incidence ranges from 1:15,000 to 1:50,000 live-born infants. The main clinical features are a high-pitched monochromatic cry, microcephaly, broad nasal bridge, epicanthal folds, micrognathia, abnormal dermatoglyphics, and severe psychomotor and mental retardation. Malformations, although not very frequent, may be present: cardiac, neurological and renal abnormalities, preauricular tags, syndactyly, hypospadias, and cryptorchidism. Molecular cytogenetic analysis has allowed a cytogenetic and phenotypic map of 5p to be defined, even if results from the studies reported up to now are not completely in agreement. Genotype-phenotype correlation studies showed a clinical and cytogenetic variability. The identification of phenotypic subsets associated with a specific size and type of deletion is of diagnostic and prognostic relevance. Specific growth and psychomotor development charts have been established. Two genes, Semaphorin F (\n                    <jats:italic>SEMAF<\/jats:italic>\n                    ) and\n                    <jats:bold>\u03b4<\/jats:bold>\n                    -catenin (\n                    <jats:italic>CTNND2<\/jats:italic>\n                    ), which have been mapped to the \"critical regions\", are potentially involved in cerebral development and their deletion may be associated with mental retardation in CdCS patients. Deletion of the telomerase reverse transcriptase (\n                    <jats:italic>hTERT<\/jats:italic>\n                    ) gene, localised to 5p15.33, could contribute to the phenotypic changes in CdCS. The critical regions were recently refined by using array comparative genomic hybridisation. The cat-like cry critical region was further narrowed using quantitative polymerase chain reaction (PCR) and three candidate genes were characterised in this region. The diagnosis is based on typical clinical manifestations. Karyotype analysis and, in doubtful cases, FISH analysis will confirm the diagnosis. There is no specific therapy for CdCS but early rehabilitative and educational interventions improve the prognosis and considerable progress has been made in the social adjustment of CdCS patients.\n                  <\/jats:p>","DOI":"10.1186\/1750-1172-1-33","type":"journal-article","created":{"date-parts":[[2006,9,5]],"date-time":"2006-09-05T14:32:02Z","timestamp":1157466722000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":181,"title":["Cri du Chat syndrome"],"prefix":"10.1186","volume":"1","author":[{"given":"Paola","family":"Cerruti Mainardi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2006,9,5]]},"reference":[{"key":"33_CR1","first-page":"3098","volume":"257","author":"J Lejeune","year":"1963","unstructured":"Lejeune J, Lafourcade J, Berger R, Vialatte J, Boeswillwald M, Seringe P, Turpin R: Trois cas de d\u00e9l\u00e9tion partielle du bras court d'un chromosome 5. CR Acad Sci (D). 1963, 257: 3098-3102.","journal-title":"CR Acad Sci (D)"},{"key":"33_CR2","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1093\/hmg\/3.2.247","volume":"3","author":"J Overhauser","year":"1994","unstructured":"Overhauser J, Huang X, Gersh M, Wilson W, McMahon J, Bengtsson U, Rojas K, Meyer M, Wasmuth JJ: Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndrome. Hum Mol Genet. 1994, 3: 247-252.","journal-title":"Hum Mol Genet"},{"key":"33_CR3","doi-asserted-by":"crossref","first-page":"295","DOI":"10.1093\/hmg\/4.2.295","volume":"4","author":"AD Simmons","year":"1995","unstructured":"Simmons AD, Goodard SA, Gallardo TD, Overhauser J, Lovett M: Five novel genes from the cri-du-chat critical region isolated by direct selection. Hum Mol Genet. 1995, 4: 295-302.","journal-title":"Hum Mol Genet"},{"key":"33_CR4","doi-asserted-by":"crossref","first-page":"770","DOI":"10.1016\/S0387-7604(12)80004-0","volume":"12","author":"M Higurashi","year":"1990","unstructured":"Higurashi M, Oda M, Iijima K, Iijima S, Takeshita T, Watanabe N, Yoneyama K: Livebirths prevalence and follow-up of malformation syndromes in 27,472 newborns. Brain Dev. 1990, 12: 770-773.","journal-title":"Brain Dev"},{"key":"33_CR5","doi-asserted-by":"publisher","first-page":"227","DOI":"10.1007\/BF00394291","volume":"44","author":"E Niebuhr","year":"1978","unstructured":"Niebuhr E: The cri du chat syndrome. Epidemiology, cytogenetics and clinical features. Hum Genet. 1978, 44: 227-275. 10.1007\/BF00394291.","journal-title":"Hum Genet"},{"key":"33_CR6","first-page":"303","volume":"3","author":"AC Duarte","year":"2004","unstructured":"Duarte AC, Cunha E, Roth JM, Ferriera FL, Garcias GL, Martino-Roth MG: Cytogenetics of genetic counseling patients in Pelotas, Rio Grande do Sul, Brazil. Genet Mol Res. 2004, 3: 303-308.","journal-title":"Genet Mol Res"},{"key":"33_CR7","first-page":"416","volume-title":"La patologia cromosomica \u2013 Atti dei Congressi della Societ\u00e0 Italiana di Medicina Interna, 74\u00b0 Congresso, Montecatini, 21\u201324 ottobre","author":"B Dallapiccola","year":"1973","unstructured":"Dallapiccola B: Malattia del \"cri du chat\" (5p-). La patologia cromosomica \u2013 Atti dei Congressi della Societ\u00e0 Italiana di Medicina Interna, 74\u00b0 Congresso, Montecatini, 21\u201324 ottobre. 1973, Roma: L. Pozzi, 416-436."},{"key":"33_CR8","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1017\/S1120962300017571","volume":"22","author":"B Dallapiccola","year":"1973","unstructured":"Dallapiccola B, Pistocchi G, Forabosco A, Capra L: Skeletal changes in the \"cri du chat\" syndrome. Acta Genet Med Gemellol. 1973, 22: 39-44.","journal-title":"Acta Genet Med Gemellol"},{"key":"33_CR9","first-page":"2389","volume":"28","author":"P Cerruti Mainardi","year":"1976","unstructured":"Cerruti Mainardi P, Vianello MG, Bonioli E: Considerazioni su 5 casi di sindrome di \"cri du chat\". Minerva Pediatr. 1976, 28: 2389-2400.","journal-title":"Minerva Pediatr"},{"key":"33_CR10","doi-asserted-by":"publisher","first-page":"528","DOI":"10.1016\/S0022-3476(83)80179-6","volume":"102","author":"LE Wilkins","year":"1983","unstructured":"Wilkins LE, Brown JA, Nance WE, Wolf B: Clinical heterogeneity in 80 home-reared children with cri-du-chat syndrome. J Pediatr. 1983, 102: 528-533. 10.1016\/S0022-3476(83)80179-6.","journal-title":"J Pediatr"},{"key":"33_CR11","volume-title":"Catalogue of unbalanced chromosome aberrations in man","author":"A Schinzel","year":"1984","unstructured":"Schinzel A: Catalogue of unbalanced chromosome aberrations in man Berlin: Walter de Gruyter; 1984."},{"key":"33_CR12","first-page":"251","volume":"37","author":"V Benigno","year":"1985","unstructured":"Benigno V, Cammarata M, Giuffr\u00e8 L: La sindrome del \"cri du chat\": dermatoglifi palmari di interesse diagnostico. Minerva Pediatr. 1985, 37: 251-253.","journal-title":"Minerva Pediatr"},{"key":"33_CR13","first-page":"281","volume":"29","author":"K Fenger","year":"1985","unstructured":"Fenger K, Niebuhr E: Discriminant analysis of dermatoglyphic sole and palm patterns in Danish cri du chat probands and normal controls. J Ment Defic Res. 1985, 29: 281-288.","journal-title":"J Ment Defic Res"},{"key":"33_CR14","first-page":"113","volume-title":"Patologia genetica ad esordio tardivo","author":"P Cerruti Mainardi","year":"1987","unstructured":"Cerruti Mainardi P: La sindrome del cri du chat in et\u00e0 adulta. Patologia genetica ad esordio tardivo. Edited by: Andria G, Dagna Bricarelli F, Del Porto G, De Marchi M, Federico A. Bologna: Monduzzi; 1987:113-128."},{"key":"33_CR15","first-page":"89","volume-title":"Malattie da aberrazioni cromosomiche","author":"L Bruni","year":"1988","unstructured":"Bruni L: La sindrome 5p-(sindrome del \"cri du chat\"). Malattie da aberrazioni cromosomiche. Edited by: Vignetti P, Ferrante E. Torino: Edizioni Minerva Medica Italia; 1988, 89-94."},{"key":"33_CR16","first-page":"254","volume-title":"Difetti congeniti e sindromi malformative","author":"B Dallapiccola","year":"1990","unstructured":"Dallapiccola B: Sindrome del \"cri du chat\". Difetti congeniti e sindromi malformative. Edited by: Mastroiacovo P, Dallapiccola B, Andria G, Camera G, Lungarotti MS. Milano: McGraw Hill Libri Italia; 1990, 254-255."},{"key":"33_CR17","first-page":"75","volume-title":"Linee guida assistenziali nel bambino con sindrome malformativa","author":"P Cerruti Mainardi","year":"1994","unstructured":"Cerruti Mainardi P, Pastore G, Guala A: Sindrome del cri du chat. Linee guida assistenziali nel bambino con sindrome malformativa. Edited by: Balestrazzi P. Milano: CSH; 1994, 75-90."},{"key":"33_CR18","first-page":"840","volume":"27","author":"P Cerruti Mainardi","year":"2001","unstructured":"Cerruti Mainardi P, Perfumo C, Pastore G, Cal\u00ec A, Guala A, Biroli E, Liverani ME, Egidi I, Zara F, Zerega G, Overhauser J, Pierluigi M, Dagna Bricarelli F: Cri du Chat Syndrome. Ital J Pediatr. 2001, 27: 840-850.http:\/\/www.ijp.it\/articoli\/2001\/vol6-01\/indice6_01.htm,","journal-title":"Ital J Pediatr"},{"key":"33_CR19","volume-title":"Eur J Med Genet","author":"P Cerruti Mainardi","year":"2006","unstructured":"Cerruti Mainardi P, Pastore G, Castronovo C, Godi M, Guala A, Tamiazzo S, Provera S, Pierluigi M, Dagna Bricarelli F: The natural history of Cri du Chat Syndrome. A report from the Italian Register. Eur J Med Genet 2006 in press."},{"key":"33_CR20","volume-title":"Tesi di Laurea","author":"M Rizzi","year":"1997","unstructured":"Rizzi M: Valutazione immunologica in pazienti affetti dalla sindrome del cri du chat 5p-. Tesi di Laurea. Facolt\u00e0 di Medicina e Chirurgia, Universit\u00e0 degli Studi di Milano, Anno Accademico; 1997."},{"key":"33_CR21","doi-asserted-by":"publisher","first-page":"6","DOI":"10.1002\/(SICI)1096-8628(19990101)82:1<6::AID-AJMG2>3.0.CO;2-#","volume":"82","author":"I Kjaer","year":"1999","unstructured":"Kjaer I, Niebuhr E: Studies of cranial base in 23 patients with cri-du-chat syndrome suggest a cranial developmental field involved in the condition. Am J Med Genet. 1999, 82: 6-14. 10.1002\/(SICI)1096-8628(19990101)82:1<6::AID-AJMG2>3.0.CO;2-#.","journal-title":"Am J Med Genet"},{"key":"33_CR22","doi-asserted-by":"publisher","first-page":"153","DOI":"10.1002\/1096-8628(20000911)94:2<153::AID-AJMG8>3.0.CO;2-#","volume":"94","author":"RC Marinescu","year":"2000","unstructured":"Marinescu RC, Cerruti Mainardi P, Collins MR, Kouahou M, Coucourde G, Pastore G, Eaton-Evans J, Overhauser J: Growth charts for cri-du-chat syndrome: an international collaborative study. Am J Med Genet. 2000, 94: 153-162. 10.1002\/1096-8628(20000911)94:2<153::AID-AJMG8>3.0.CO;2-#.","journal-title":"Am J Med Genet"},{"key":"33_CR23","doi-asserted-by":"publisher","first-page":"337","DOI":"10.1136\/adc.85.4.337","volume":"85","author":"MS Collins","year":"2001","unstructured":"Collins MS, Eaton-Evans J: Growth study of cri du chat syndrome. Arch Dis Child. 2001, 85: 337-338. 10.1136\/adc.85.4.337.","journal-title":"Arch Dis Child"},{"key":"33_CR24","doi-asserted-by":"crossref","first-page":"82","DOI":"10.1111\/j.1399-0004.1979.tb00856.x","volume":"16","author":"E Niebuhr","year":"1979","unstructured":"Niebuhr E: Antropometry in the Cri du Chat syndrome. Clin Genet. 1979, 16: 82-95.","journal-title":"Clin Genet"},{"key":"33_CR25","doi-asserted-by":"publisher","first-page":"782","DOI":"10.1016\/S0022-3476(70)80236-0","volume":"77","author":"WR Breg","year":"1970","unstructured":"Breg WR, Steele MW, Miller OJ, Warburtonb D, Capoa A, Allerdice PW: The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome N\u00b0 5 (5p-). J Pediatr. 1970, 77: 782-791. 10.1016\/S0022-3476(70)80236-0.","journal-title":"J Pediatr"},{"key":"33_CR26","first-page":"277","volume":"15","author":"E Niebuhr","year":"1971","unstructured":"Niebuhr E: The cat cry syndrome (5p-) in adolescents and adults. J Ment Defic Res. 1971, 15: 277-291.","journal-title":"J Ment Defic Res"},{"key":"33_CR27","doi-asserted-by":"publisher","first-page":"203","DOI":"10.1002\/(SICI)1096-8628(20000131)90:3<203::AID-AJMG5>3.0.CO;2-A","volume":"90","author":"GJCM Van Buggenhout","year":"2000","unstructured":"Van Buggenhout GJCM, Pijkels E, Holvoet M, Schaap C, Hamel BCJ, Fryns JP: Cri du Chat Syndrome: changing phenotype in older patients. Am J Med Genet. 2000, 90: 203-215. 10.1002\/(SICI)1096-8628(20000131)90:3<203::AID-AJMG5>3.0.CO;2-A.","journal-title":"Am J Med Genet"},{"key":"33_CR28","first-page":"17","volume":"16","author":"R Posmyk","year":"2005","unstructured":"Posmyk R, Panasiuk B, Yatsenko SA, Stankiewicz P, Midro AT: A natural history of a child with monosomy 5p syndrome (Cat-cry\/Cri-du-chat syndrome) during the 18 years of follow-up. Genet Couns. 2005, 16: 17-25.","journal-title":"Genet Couns"},{"key":"33_CR29","doi-asserted-by":"crossref","first-page":"949","DOI":"10.1016\/0002-9394(72)90465-5","volume":"73","author":"RO Howard","year":"1972","unstructured":"Howard RO: Ocular abnormalities in the cri du chat syndrome. Am J Ophthalmol. 1972, 73: 949-954.","journal-title":"Am J Ophthalmol"},{"key":"33_CR30","doi-asserted-by":"crossref","first-page":"304","DOI":"10.1136\/jmg.20.4.304","volume":"20","author":"S Kitsiou-Tzeli","year":"1983","unstructured":"Kitsiou-Tzeli S, Dellagrammaticas HD, Papas CB, Ladas ID, Bartsocas CS: Unusual ocular findings in an infant with cri-du-chat syndrome. J Med Genet. 1983, 20: 304-307.","journal-title":"J Med Genet"},{"key":"33_CR31","doi-asserted-by":"publisher","first-page":"68","DOI":"10.1002\/ajmg.1320460111","volume":"46","author":"L Kobrynski","year":"1993","unstructured":"Kobrynski L, Chitayat D, Zahed L, McGregor D, Rochon L, Brownstein S, Vekemans M, Albert DL: Trisomy 22 and facioauriculovertebral (Goldenhar) sequence. Am J Med Genet. 1993, 46: 68-71. 10.1002\/ajmg.1320460111.","journal-title":"Am J Med Genet"},{"key":"33_CR32","doi-asserted-by":"crossref","first-page":"226","DOI":"10.1016\/S1091-8531(02)42019-8","volume":"7","author":"YF Choong","year":"2003","unstructured":"Choong YF, Watts P, Little E, Beck L: Goldenhar and cri-du-chat syndromes: a contiguous gene deletion syndrome?. J AAPOS. 2003, 7: 226-227.","journal-title":"J AAPOS"},{"key":"33_CR33","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1111\/j.1399-0004.1994.tb04169.x","volume":"46","author":"MW McLellan","year":"1994","unstructured":"McLellan MW, Golden WL, Wilson WG: Marfan and cri du chat syndromes in an 18-month-old child: evidence of phenotype interaction. Clin Genet. 1994, 46: 319-321.","journal-title":"Clin Genet"},{"key":"33_CR34","doi-asserted-by":"publisher","first-page":"363","DOI":"10.1002\/ajmg.a.10268","volume":"119","author":"E Stathopulu","year":"2003","unstructured":"Stathopulu E, Mackie Ogilvie C, Flinter FA: Terminal deletion of chromosome 5p in a patient with phenotypical features of Lujan-Fryns syndrome. Am J Med Genet A. 2003, 119: 363-6. 10.1002\/ajmg.a.10268.","journal-title":"Am J Med Genet A"},{"key":"33_CR35","doi-asserted-by":"crossref","first-page":"212","DOI":"10.1111\/j.1399-0004.1993.tb04467.x","volume":"43","author":"JE Martinez","year":"1993","unstructured":"Martinez JE, Tuck-Muller CM, Superneau D, Wertelecki W: Fertility and cri du chat syndrome. Clin Genet. 1993, 43: 212-214.","journal-title":"Clin Genet"},{"key":"33_CR36","first-page":"75","volume":"36","author":"J Tamraz","year":"1993","unstructured":"Tamraz J, Rethor\u00e9 MO, Lejeune J, Outin C, Goepel R, Stievenart JL, Iba-Zizen MT, Cabanis EA: Morphom\u00e9trie enc\u00e9phalique en IRM dans la maladie du cri du chat. A propos de sept patients, avec revue de la litt\u00e9rature. Ann Genet. 1993, 36: 75-87.","journal-title":"Ann Genet"},{"key":"33_CR37","first-page":"92","volume":"15","author":"G De Michele","year":"1993","unstructured":"De Michele G, Presta M, Di Salle F, Serra L, Mazzaccara A, Della Rocca G, Ambrosio G, Filla A: Cerebellar vermis hypoplasia in a case of cri-du-chat syndrome. Acta Neurol (Napoli). 1993, 15: 92-6.","journal-title":"Acta Neurol (Napoli)"},{"key":"33_CR38","doi-asserted-by":"publisher","first-page":"289","DOI":"10.1097\/00019605-200110000-00011","volume":"10","author":"S Balci","year":"2001","unstructured":"Balci S, Oguz KK: Cri-du-chat syndrome associated with arachnoid cyst causing triventricular hydrocephalus. Clin Dysmorphol. 2001, 10: 289-290. 10.1097\/00019605-200110000-00011.","journal-title":"Clin Dysmorphol"},{"key":"33_CR39","first-page":"16","volume":"33","author":"J Lejeune","year":"1990","unstructured":"Lejeune J, Rethor\u00e9 MO, Peeters M, de Blois MC, Rabier D, Parvy P, Bardet J, Kamoun P: Maladie du cri du chat: acides amin\u00e9s plasmatiques et urinaires. Ann Genet. 1990, 33: 16-20.","journal-title":"Ann Genet"},{"key":"33_CR40","first-page":"219","volume":"34","author":"MA Peeters","year":"1991","unstructured":"Peeters MA, Rethor\u00e9 MO, Aris L, Megarbane A, Cattaneo F, Lejeune J: Metabolic anomalies in cri du chat syndrome (5p-) lymphocytes and the novo purine synthesis. Ann Genet. 1991, 34: 219-225.","journal-title":"Ann Genet"},{"key":"33_CR41","doi-asserted-by":"publisher","first-page":"198","DOI":"10.1002\/ajmg.a.30592","volume":"134","author":"CY Tsao","year":"2005","unstructured":"Tsao CY, Wenger GD, Bartholomew DW: Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopia. Am J Med Genet A. 2005, 134: 198-201. 10.1002\/ajmg.a.30592.","journal-title":"Am J Med Genet A"},{"key":"33_CR42","doi-asserted-by":"publisher","first-page":"401","DOI":"10.1016\/S0022-3476(80)80189-2","volume":"97","author":"LE Wilkins","year":"1980","unstructured":"Wilkins LE, Brown JA, Wolf B: Psychomotor development in 65 home-reared children with cri-du-chat syndrome. J Pediatr. 1980, 97: 401-405. 10.1016\/S0022-3476(80)80189-2.","journal-title":"J Pediatr"},{"key":"33_CR43","first-page":"64","volume-title":"Procedings of the 8th Congress of International Association for the Scientific Study of Mental Deficiency","author":"ME Carlin","year":"1990","unstructured":"Carlin ME: The improved prognosis in cri-du-chat (5p-) syndrome. Procedings of the 8th Congress of International Association for the Scientific Study of Mental Deficiency. Edited by: Fraser W. 1990, Edinburgh: Blackwell, 64-73."},{"key":"33_CR44","doi-asserted-by":"crossref","first-page":"448","DOI":"10.1136\/adc.75.5.448","volume":"75","author":"KM Cornish","year":"1996","unstructured":"Cornish KM, Pigram J: Developmental and behavioural characteristics of cri du chat syndrome. Arch Dis Child. 1996, 75: 448-450.","journal-title":"Arch Dis Child"},{"key":"33_CR45","doi-asserted-by":"publisher","first-page":"73","DOI":"10.1016\/S0021-9924(97)00052-X","volume":"31","author":"KM Cornish","year":"1998","unstructured":"Cornish KM, Munir F: Receptive and expressive speech skills in children with cri-du-chat syndrome. J Commun Disord. 1998, 31: 73-80. 10.1016\/S0021-9924(97)00052-X.","journal-title":"J Commun Disord"},{"issue":"4","key":"33_CR46","doi-asserted-by":"publisher","first-page":"263","DOI":"10.1017\/S0012162299000559","volume":"41","author":"KM Cornish","year":"1999","unstructured":"Cornish KM, Bramble D, Munir F, Pigram J: Cognitive functioning in children with typical cri du chat (5p-) syndrome. Dev Med Child Neurol. 1999, 41 (4): 263-6. 10.1017\/S0012162299000559.","journal-title":"Dev Med Child Neurol"},{"key":"33_CR47","doi-asserted-by":"publisher","first-page":"459","DOI":"10.1034\/j.1399-0004.2000.570612.x","volume":"57","author":"P Cerruti Mainardi","year":"2000","unstructured":"Cerruti Mainardi P, Guala A, Pastore G, Pozzo G, Dagna Bricarelli F, Pierluigi M: Psychomotor development in cri du chat syndrome. Clin Genet. 2000, 57: 459-461. 10.1034\/j.1399-0004.2000.570612.x.","journal-title":"Clin Genet"},{"key":"33_CR48","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1542\/peds.89.1.91","volume":"89","author":"WK Frankenburg","year":"1992","unstructured":"Frankenburg WK, Dodds JB, Archer P, Shapiro H, Bresnick B: The Denver II: a major revision restandardization of the Denver Developmental Screening Test. Pediatrics. 1992, 89: 91-97.","journal-title":"Pediatrics"},{"key":"33_CR49","doi-asserted-by":"crossref","first-page":"752","DOI":"10.1111\/j.1469-8749.1997.tb07377.x","volume":"39","author":"EM Dykens","year":"1997","unstructured":"Dykens EM, Clarke DJ: Correlates of maladaptive behaviour in individuals with 5p- (cri du chat) syndrome. Dev Med Child Neurol. 1997, 39: 752-756.","journal-title":"Dev Med Child Neurol"},{"key":"33_CR50","doi-asserted-by":"publisher","first-page":"264","DOI":"10.1352\/0895-8017(1998)103<0264:PBAWDP>2.0.CO;2","volume":"103","author":"DJ Clarke","year":"1998","unstructured":"Clarke DJ, Boer H: Problem behaviours associated with deletion Prader-Willi, Smith-Magenis, and Cri du Chat Syndromes. Am J Ment Retard. 1998, 103: 264-271. 10.1352\/0895-8017(1998)103<0264:PBAWDP>2.0.CO;2.","journal-title":"Am J Ment Retard"},{"key":"33_CR51","doi-asserted-by":"publisher","first-page":"133","DOI":"10.1046\/j.1365-2788.2002.00361.x","volume":"46","author":"MS Collins","year":"2002","unstructured":"Collins MS, Cornish K: A survey of the prevalence of stereotypy, self-injury and aggression in children and young adults with Cri du Chat syndrome. J Intellect Disabil Res. 2002, 46: 133-140. 10.1046\/j.1365-2788.2002.00361.x.","journal-title":"J Intellect Disabil Res"},{"key":"33_CR52","doi-asserted-by":"publisher","first-page":"113","DOI":"10.1046\/j.1365-2788.2003.00448.x","volume":"47","author":"K Sarimski","year":"2003","unstructured":"Sarimski K: Early play behaviour in children with 5p- (Cri-du-Chat) syndrome. J Intellect Disabil Res. 2003, 47: 113-120. 10.1046\/j.1365-2788.2003.00448.x.","journal-title":"J Intellect Disabil Res"},{"key":"33_CR53","first-page":"1404","volume":"56","author":"M Gersh","year":"1995","unstructured":"Gersh M, Goodart SA, Pasztor LM, Harris DJ, Weiss L, Overhauser J: Evidence for a distinct region causing a cat-like cry in patients with 5p deletions. Am J Hum Genet. 1995, 56: 1404-1410.","journal-title":"Am J Hum Genet"},{"key":"33_CR54","first-page":"1162","volume":"56","author":"DM Church","year":"1995","unstructured":"Church DM, Bengtsson U, Nielsen KV, Wasmuth JJ, Niebuhr E: Molecular definition of deletions of different segments of distal 5p that result in distinct phenotypic features. Am J Hum Genet. 1995, 56: 1162-1172.","journal-title":"Am J Hum Genet"},{"key":"33_CR55","doi-asserted-by":"crossref","first-page":"787","DOI":"10.1101\/gr.7.8.787","volume":"7","author":"DM Church","year":"1997","unstructured":"Church DM, Yang J, Bocian M, Shiang R, Wasmuth JJ: A high-resolution physical and transcript map of the Cri du Chat region of human chromosome 5p. Genome Res. 1997, 7: 787-801.","journal-title":"Genome Res"},{"key":"33_CR56","doi-asserted-by":"publisher","first-page":"151","DOI":"10.1136\/jmg.38.3.151","volume":"38","author":"P Cerruti Mainardi","year":"2001","unstructured":"Cerruti Mainardi P, Perfumo C, Cal\u00ec A, Coucourde G, Pastore G, Cavani S, Zara F, Overhauser J, Pierluigi M, Dagna Bricarelli F: Clinical and molecular characterization of 80 patients with 5p deletion: genotype \u2013 phenotype correlation. J Med Genet. 2001, 38: 151-158. 10.1136\/jmg.38.3.151.","journal-title":"J Med Genet"},{"key":"33_CR57","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1101\/gr.7.2.118","volume":"7","author":"AD Simmons","year":"1997","unstructured":"Simmons AD, Overhauser J, Lovett M: Isolation of cDNAs from the Cri-du-chat critical region by direct screening of a chromosome 5-specific cDNA library. Genome Res. 1997, 7: 118-127.","journal-title":"Genome Res"},{"key":"33_CR58","doi-asserted-by":"publisher","first-page":"83","DOI":"10.1002\/ajmg.1320370119","volume":"37","author":"J Overhauser","year":"1990","unstructured":"Overhauser J, McMahon J, Oberlender S, Carlin ME, Niebuhr E, Wasmuth JJ, Lee-chen J: Parental origin of chromosome 5 deletions in the cri du chat syndrome. Am J Med Genet. 1990, 37: 83-86. 10.1002\/ajmg.1320370119.","journal-title":"Am J Med Genet"},{"key":"33_CR59","doi-asserted-by":"publisher","first-page":"157","DOI":"10.1006\/geno.1999.6090","volume":"63","author":"M Medina","year":"2000","unstructured":"Medina M, Marinescu RC, Overhauser J, Kosik SK: Hemizigosity of delta-catenin (CTNND2) is associated with severe mental retardation in cri-du-chat syndrome. Genomics. 2000, 63: 157-164. 10.1006\/geno.1999.6090.","journal-title":"Genomics"},{"key":"33_CR60","first-page":"776","volume":"A136","author":"J Overhauser","year":"1997","unstructured":"Overhauser J, Marinescu RC, Cheung M, Simmons A, Wixted D, Robin NH, Lovett M: Mapping of genes within a reduced cri-du-chat critical region [abstract]. Am J Hum Genet. 1997, A136: 776.","journal-title":"Am J Hum Genet"},{"key":"33_CR61","doi-asserted-by":"crossref","first-page":"1225","DOI":"10.1093\/hmg\/4.7.1225","volume":"4","author":"AE Hughes","year":"1995","unstructured":"Hughes AE, McGibbon D, Woodward E, Dixey J, Doherty M: Localization of a gene for chondrocalcinosis to chromosome 5p. Hum Mol Genet. 1995, 4: 1225-1228.","journal-title":"Hum Mol Genet"},{"key":"33_CR62","doi-asserted-by":"publisher","first-page":"389","DOI":"10.1038\/ng0497-389","volume":"15","author":"The Collaborative Study of the Genetics of Asthma","year":"1997","unstructured":"The Collaborative Study of the Genetics of Asthma. A genome-wide search for asthma susceptibility loci in ethnically diverse populations. Nature Genet. 1997, 15: 389-392. 10.1038\/ng0497-389.","journal-title":"Nature Genet"},{"key":"33_CR63","doi-asserted-by":"publisher","first-page":"685","DOI":"10.1006\/bbrc.1997.8027","volume":"242","author":"AD Simmons","year":"1998","unstructured":"Simmons AD, Pueschel AW, Mc Pherson JD, Overhauser J, Lovett M: Molecular cloning and mapping of human Semaphorin F from the Cri-du-Chat candidate interval. Biochem Biophys Res Com. 1998, 242: 685-691. 10.1006\/bbrc.1997.8027.","journal-title":"Biochem Biophys Res Com"},{"key":"33_CR64","doi-asserted-by":"publisher","first-page":"1657","DOI":"10.1016\/j.cub.2004.08.065","volume":"14","author":"I Israely","year":"2004","unstructured":"Israely I, Costa RM, Xie CW, Silva AJ, Kosik KS, Liu X: Deletion of the neuron-specific protein delta-catenin leads to severe cognitive and synaptic dysfunction. Curr Biol. 2004, 14: 1657-1663. 10.1016\/j.cub.2004.08.065.","journal-title":"Curr Biol"},{"key":"33_CR65","doi-asserted-by":"publisher","first-page":"940","DOI":"10.1086\/374565","volume":"72","author":"A Zhang","year":"2003","unstructured":"Zhang A, Zheng C, Hou M, Lindvall C, Li K, Erlandsson F, Bj\u00f6rkholm M, Gruber A, Blennow E, Xu D: Deletion of the telomerase reverse transcriptase gene and haploinsufficiency of telomere maintenance in Cri du chat syndrome. Am J Hum Genet. 2003, 72: 940-948. 10.1086\/374565.","journal-title":"Am J Hum Genet"},{"issue":"1","key":"33_CR66","doi-asserted-by":"publisher","first-page":"66","DOI":"10.1002\/(SICI)1096-8628(19990903)86:1<71::AID-AJMG14>3.0.CO;2-Y","volume":"86","author":"RC Marinescu","year":"1999","unstructured":"Marinescu RC, Johnson EI, Dykens EM, Hodapp RM, Overhauser J: No relationship between the size of the deletion and the level of developmental delay in cri-du-chat syndrome. Am J Med Genet. 1999, 86 (1): 66-70. 10.1002\/(SICI)1096-8628(19990903)86:1<71::AID-AJMG14>3.0.CO;2-Y.","journal-title":"Am J Med Genet"},{"key":"33_CR67","first-page":"567","volume":"36","author":"KM Cornish","year":"1999","unstructured":"Cornish KM, Cross G, Green A, Willatt L, Bradsh JM: A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosis. J Med Genet. 1999, 36: 567-570.","journal-title":"J Med Genet"},{"key":"33_CR68","doi-asserted-by":"publisher","first-page":"143","DOI":"10.1007\/BF00283634","volume":"42","author":"E Niebuhr","year":"1978","unstructured":"Niebuhr E: Cytologic observations in 35 individuals with a 5p-karyotype. Hum Genet. 1978, 42: 143-146. 10.1007\/BF00283634.","journal-title":"Hum Genet"},{"key":"33_CR69","doi-asserted-by":"publisher","first-page":"389","DOI":"10.1007\/BF00569228","volume":"60","author":"C Baccichetti","year":"1982","unstructured":"Baccichetti C: Del(5p) without \"cri du chat\" phenotype [abstract]. Hum Genet. 1982, 60: 389-10.1007\/BF00569228.","journal-title":"Hum Genet"},{"key":"33_CR70","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1111\/j.1399-0004.1988.tb02868.x","volume":"34","author":"C Baccichetti","year":"1988","unstructured":"Baccichetti C, Lenzini E, Artifoni L, Caufin D, Marangoni P: Terminal deletion of the short arm of chromosome 5. Clin Genet. 1988, 34: 219-223.","journal-title":"Clin Genet"},{"key":"33_CR71","first-page":"1","volume":"39","author":"J Overhauser","year":"1986","unstructured":"Overhauser J, Golbus MS, Schonberg SA, Wasmuth JJ: Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype. Am J Hum Genet. 1986, 39: 1-10.","journal-title":"Am J Hum Genet"},{"key":"33_CR72","first-page":"145","volume":"A753","author":"P Cerruti Mainardi","year":"2000","unstructured":"Cerruti Mainardi P, Cal\u00ec A, Guala A, Perfumo C, Liverani ME, Pastore G, Overhauser J, Zara F, Pierluigi M, Dagna Bricarelli F: Phenotype-genotype correlation in 7 patients with 5p\/autosome translocations. Risk for carriers of translocations involving 5p [abstract]. Am J Hum Genet. 2000, A753: 145.","journal-title":"Am J Hum Genet"},{"key":"33_CR73","doi-asserted-by":"publisher","first-page":"967","DOI":"10.1136\/jmg.37.12.967","volume":"37","author":"C Perfumo","year":"2000","unstructured":"Perfumo C, Cerruti Mainardi P, Cal\u00ec A, Coucourde G, Zara F, Cavani S, Overhauser J, Dagna Bricarelli F, Pierluigi M: The first three mosaic cri du chat syndrome patients with two rearranged cell lines. J Med Genet. 2000, 37: 967-972. 10.1136\/jmg.37.12.967.","journal-title":"J Med Genet"},{"key":"33_CR74","doi-asserted-by":"publisher","first-page":"578","DOI":"10.1002\/pd.906","volume":"24","author":"S Kitsiou","year":"2004","unstructured":"Kitsiou S, Kolialexi A, Mavrou A: Mosaic Cri du Chat syndrome in a patient exhibiting three 5p cell lines. Prenat Diagn. 2004, 24: 578-579. 10.1002\/pd.906.","journal-title":"Prenat Diagn"},{"key":"33_CR75","doi-asserted-by":"publisher","first-page":"192","DOI":"10.1002\/ajmg.10261","volume":"108","author":"B Levy","year":"2002","unstructured":"Levy B, Dunn TM, Kern JH, Hirschhorn K, Kardon NB: Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q\/del 5p (cri du chat). Am J Med Genet. 2002, 108: 192-197. 10.1002\/ajmg.10261.","journal-title":"Am J Med Genet"},{"key":"33_CR76","doi-asserted-by":"publisher","first-page":"189","DOI":"10.1002\/ajmg.a.30519","volume":"133","author":"E Rossi","year":"2005","unstructured":"Rossi E, De Gregori M, Patricelli MG, Pramparo T, Argentiero L, Giglio S, Sosta K, Foresti G, Zuffardi O: 8.5 Mb deletion at distal 5p in a male ascertained for azoospermia. Am J Med Genet A. 2005, 133: 189-192. 10.1002\/ajmg.a.30519.","journal-title":"Am J Med Genet A"},{"key":"33_CR77","doi-asserted-by":"publisher","first-page":"312","DOI":"10.1086\/427762","volume":"76","author":"X Zhang","year":"2005","unstructured":"Zhang X, Snijders A, Segraves R, Zhang X, Niebuhr A, Albertson D, Yang H, Gray J, Niebuhr E, Bolund L, Pinkel D: High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization. Am J Hum Genet. 2005, 76: 312-326. 10.1086\/427762.","journal-title":"Am J Hum Genet"},{"key":"33_CR78","doi-asserted-by":"publisher","first-page":"475","DOI":"10.1038\/sj.ejhg.5201345","volume":"13","author":"Q Wu","year":"2005","unstructured":"Wu Q, Niebuhr E, Yang H, Hansen L: Determination of the 'critical region' for cat-like cry of Cri-du-chat syndrome and analysis of candidate genes by quantitative PCR. Eur J Hum Genet. 2005, 13: 475-485. 10.1038\/sj.ejhg.5201345.","journal-title":"Eur J Hum Genet"},{"key":"33_CR79","doi-asserted-by":"publisher","first-page":"341","DOI":"10.1111\/j.1399-0004.2005.00406.x","volume":"67","author":"C Harvard","year":"2005","unstructured":"Harvard C, Malenfant P, Koochek M, Creighton S, Mickelson EC, Holden JJ, Lewis ME, Rajcan-Separovic E: A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH. Clin Genet. 2005, 67: 341-351. 10.1111\/j.1399-0004.2005.00406.x.","journal-title":"Clin Genet"},{"key":"33_CR80","doi-asserted-by":"publisher","first-page":"282","DOI":"10.1034\/j.1399-0004.1999.560405.x","volume":"56","author":"RC Marinescu","year":"1999","unstructured":"Marinescu RC, Johnson EI, Grady D, Chen XN, Overhauser J: FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome. Clin Genet. 1999, 56: 282-288. 10.1034\/j.1399-0004.1999.560405.x.","journal-title":"Clin Genet"},{"key":"33_CR81","doi-asserted-by":"publisher","first-page":"51","DOI":"10.1007\/s004390050010","volume":"107","author":"M Granzow","year":"2000","unstructured":"Granzow M, Popp S, Keller M, Holtgreve-Grez H, Brough M, Schoell B, Rauterberg-Ruland I, Hager HD, Tariverdian G, Jauch A: Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individuals. Hum Genet. 2000, 107: 51-57. 10.1007\/s004390050010.","journal-title":"Hum Genet"},{"key":"33_CR82","doi-asserted-by":"publisher","first-page":"86","DOI":"10.1002\/ajmg.a.20420","volume":"125","author":"R Ensenauer","year":"2004","unstructured":"Ensenauer R, Jalal S, Meyer R, Babovic-Vuksanovic D: Unbalanced cryptic 5p deletion\/17p duplication identified by subtelomeric FISH in a family with a boy with chimerism and a balanced t(4;5). Am J Med Genet A. 2004, 125: 86-91. 10.1002\/ajmg.a.20420.","journal-title":"Am J Med Genet A"},{"key":"33_CR83","doi-asserted-by":"publisher","first-page":"26","DOI":"10.1007\/s10038-004-0213-9","volume":"50","author":"T Kondoh","year":"2005","unstructured":"Kondoh T, Shimokawa O, Harada N, Doi T, Yun C, Gohda Y, Kinoshita F, Matsumoto H, Moriuchi H: Genotype-phenotype correlation of 5p-syndrome: pitfall of diagnosis. J Hum Genet. 2005, 50: 26-29. 10.1007\/s10038-004-0213-9.","journal-title":"J Hum Genet"},{"key":"33_CR84","first-page":"449","volume":"70","author":"PA Benn","year":"1987","unstructured":"Benn PA, Hsu LYF, Verma RS, Aloiso ML, Reich E, Wishnick M: Prenatal diagnosis of minute 5p-deletion: a cytogenetic problem in detection. Obstet Gynecol. 1987, 70: 449-452.","journal-title":"Obstet Gynecol"},{"key":"33_CR85","doi-asserted-by":"crossref","first-page":"505","DOI":"10.1002\/pd.1970090708","volume":"9","author":"RD Smart","year":"1989","unstructured":"Smart RD, Retief AE, Overhauser J: Confirmation of a balanced chromosomal translocation using molecular techniques. Prenat Diagn. 1989, 9: 505-513.","journal-title":"Prenat Diagn"},{"key":"33_CR86","doi-asserted-by":"publisher","first-page":"77","DOI":"10.1002\/ajmg.1320460113","volume":"46","author":"R Bernstein","year":"1993","unstructured":"Bernstein R, Bocain ME, Cain MJ, Bengtsson U, Wasmuth JJ: Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization. Am J Med Genet. 1993, 46: 77-82. 10.1002\/ajmg.1320460113.","journal-title":"Am J Med Genet"},{"key":"33_CR87","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1111\/j.1399-0004.1994.tb03983.x","volume":"45","author":"MJ Pettenati","year":"1994","unstructured":"Pettenati MJ, Hayworth R, Cox K, Rao PN: Prenatal detection of cri du chat syndrome on uncultered amniocytes using fluorescence in situ hybridization (FISH). Clin Genet. 1994, 45: 17-20.","journal-title":"Clin Genet"},{"key":"33_CR88","doi-asserted-by":"publisher","first-page":"50","DOI":"10.1002\/pd.794","volume":"24","author":"CC Chen","year":"2004","unstructured":"Chen CC, Lee CC, Chang TY, Town DD, Wang W: Prenatal diagnosis of mosaic distal 5p deletion and review of the literature. Prenat Diagn. 2004, 24: 50-57. 10.1002\/pd.794.","journal-title":"Prenat Diagn"},{"key":"33_CR89","first-page":"101","volume":"44","author":"MS Tullu","year":"1998","unstructured":"Tullu MS, Muranjan MN, Sharma SV, Sahu DR, Swami SR, Deshmukh CT, Bharucha BA: Cri-du-chat syndrome: clinical profile and prenatal diagnosis. J Postgrad Med. 1998, 44: 101-104.","journal-title":"J Postgrad Med"},{"key":"33_CR90","doi-asserted-by":"publisher","first-page":"216","DOI":"10.1046\/j.1469-0705.1999.13030216.x","volume":"13","author":"S Aoky","year":"1999","unstructured":"Aoky S, Hata T, Hata K, Miyazaki K: Antenatal sonographic features of cri du chat syndrome. Ultrasound Obstet Gynecol. 1999, 13: 216-219. 10.1046\/j.1469-0705.1999.13030216.x.","journal-title":"Ultrasound Obstet Gynecol"},{"key":"33_CR91","doi-asserted-by":"publisher","first-page":"64","DOI":"10.1002\/pd.243","volume":"22","author":"EG Stefanou","year":"2002","unstructured":"Stefanou EG, Hanna G, Foakes A, Crocker M, Fitchett M: Prenatal diagnosis of cri du chat (5p) syndrome in association with isolated moderate bilateral ventriculomegaly. Prenat Diagn. 2002, 22: 64-66. 10.1002\/pd.243.","journal-title":"Prenat Diagn"},{"key":"33_CR92","doi-asserted-by":"crossref","first-page":"1614","DOI":"10.1016\/S0002-9378(11)90448-7","volume":"169","author":"AP Sarno Jr","year":"1993","unstructured":"Sarno AP, Polzin WJ, Kalish VB: Fetal choroid plexus in association with cri du chat (5p-) syndrome. Am J Obstet Gynecol. 1993, 169: 1614-5.","journal-title":"Am J Obstet Gynecol"},{"key":"33_CR93","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1002\/pd.1970130106","volume":"13","author":"F Muller","year":"1993","unstructured":"Muller F, Aegerter P, Boue A: Prospective maternal serum chorionic gonadotropin screening for the risk of fetal chromosome anomalies and of subsequent fetal and neonatal deaths. Prenat Diagn. 1993, 13: 29-43.","journal-title":"Prenat Diagn"},{"issue":"10","key":"33_CR94","doi-asserted-by":"publisher","first-page":"1099","DOI":"10.1002\/(SICI)1097-0223(1998100)18:10<1099::AID-PD400>3.0.CO;2-H","volume":"18","author":"L Fankhauser","year":"1998","unstructured":"Fankhauser L, Brundler AM, Dahoun S: Cri-du-chat syndrome diagnosed by amniocentesis performed due to abnormal maternal serum test. Prenat Diagn. 1998, 18 (10): 1099-100. 10.1002\/(SICI)1097-0223(1998100)18:10<1099::AID-PD400>3.0.CO;2-H.","journal-title":"Prenat Diagn"},{"key":"33_CR95","doi-asserted-by":"publisher","first-page":"572","DOI":"10.1002\/pd.645","volume":"23","author":"A Weiss","year":"2003","unstructured":"Weiss A, Shalev S, Weiner E, Shneor Y, Shalev E: Prenatal diagnosis of 5p deletion syndrome following abnormally low maternal serum human chorionic gonadotrophin. Prenat Diagn. 2003, 23: 572-574. 10.1002\/pd.645.","journal-title":"Prenat Diagn"},{"key":"33_CR96","doi-asserted-by":"publisher","first-page":"311","DOI":"10.1002\/pd.1130","volume":"25","author":"F Vialard","year":"2005","unstructured":"Vialard F, Robyr R, Hillion Y, Molina Gomes D, Selva J, Ville Y: Dandy-Walker syndrome and corpus callosum agenesis in 5p deletion. Prenat Diagn. 2005, 25: 311-313. 10.1002\/pd.1130.","journal-title":"Prenat Diagn"},{"key":"33_CR97","doi-asserted-by":"crossref","first-page":"472","DOI":"10.1111\/j.1399-0004.1984.tb01091.x","volume":"26","author":"T Kushnick","year":"1984","unstructured":"Kushnick T, Rao KW, Lamb AN: Familial 5p-syndrome. Clin Genet. 1984, 26: 472-476.","journal-title":"Clin Genet"},{"key":"33_CR98","first-page":"208","volume":"A47","author":"U Bengtsson","year":"1990","unstructured":"Bengtsson U, McMahon J, Quarrel Q, Rubenstein C, David K, Greenberg F, Wasmuth JJ: Phenotypically normal carriers of unbalanced terminal deletion of 5p transmit deletions to offspring who display growth and developmental delay [abstract]. Am J Hum Genet. 1990, A47: 208.","journal-title":"Am J Hum Genet"},{"key":"33_CR99","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1097\/00000542-198508000-00017","volume":"63","author":"M Yamashita","year":"1985","unstructured":"Yamashita M, Tanioka F, Taniguchi K, Maisuki A, Oyama T: Anesthetic considerations in cri du chat syndrome: a report of three cases. Anesthesiology. 1985, 63: 201-202.","journal-title":"Anesthesiology"},{"key":"33_CR100","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1111\/j.1460-9592.1995.tb00262.x","volume":"5","author":"RP Brislin","year":"1995","unstructured":"Brislin RP, Stayer SA, Schwartz RE: Anaesthetic considerations for the patient with cri du chat syndrome. Paediatr Anaesth. 1995, 5: 139-141.","journal-title":"Paediatr Anaesth"},{"key":"33_CR101","volume-title":"La Sindrome del Cri du Chat","author":"P Cerruti Mainardi","year":"2002","unstructured":"Cerruti Mainardi P, Medolago LM, Pedrinazzi M: La Sindrome del Cri du Chat. 2002, Firenze: Grafiche Borri, S. Casciano V.P,http:\/\/www.criduchat.it\/cdc\/doc_vari\/ABCLibrettoSCDC72\/ABClibrettoSCDC72.pdf,"}],"container-title":["Orphanet Journal of Rare Diseases"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1186\/1750-1172-1-33.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,6]],"date-time":"2024-02-06T04:23:41Z","timestamp":1707193421000},"score":1,"resource":{"primary":{"URL":"https:\/\/ojrd.biomedcentral.com\/articles\/10.1186\/1750-1172-1-33"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2006,9,5]]},"references-count":101,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2006,12]]}},"alternative-id":["33"],"URL":"https:\/\/doi.org\/10.1186\/1750-1172-1-33","relation":{},"ISSN":["1750-1172"],"issn-type":[{"value":"1750-1172","type":"electronic"}],"subject":[],"published":{"date-parts":[[2006,9,5]]},"assertion":[{"value":"20 July 2006","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"5 September 2006","order":2,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"5 September 2006","order":3,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}}],"article-number":"33"}}