{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,8]],"date-time":"2026-06-08T22:24:11Z","timestamp":1780957451145,"version":"3.54.1"},"reference-count":73,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[1987,2,1]],"date-time":"1987-02-01T00:00:00Z","timestamp":539136000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Hum Genet"],"published-print":{"date-parts":[[1987,2]]},"DOI":"10.1007\/bf00591068","type":"journal-article","created":{"date-parts":[[2004,11,23]],"date-time":"2004-11-23T06:37:54Z","timestamp":1101191874000},"page":"101-108","source":"Crossref","is-referenced-by-count":16,"title":["Homozygous paracentric inversion 12 in a mentally retarded boy: a case report and review of the literature"],"prefix":"10.1007","volume":"75","author":[{"given":"Hilary A.","family":"Price","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Selwyn H.","family":"Roberts","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K. Michael","family":"Laurence","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"655","DOI":"10.1139\/g80-072","volume":"22","author":"PW Allderdice","year":"1980","unstructured":"Allderdice PW, Sreenivasan U, Eales B (1980) 46,XY,inv(10) (q11q26) in a boy with normal intelligence and minor physical anomalies. Can J Genet Cytol 22:655","journal-title":"Can J Genet Cytol"},{"key":"CR2","first-page":"74","volume":"21","author":"HN Bass","year":"1978","unstructured":"Bass HN, Sparkes RS, Crandall BF, Tannenbaum SM (1978) Familial partial trisomy 10q(q23?qter) syndrome and paracentric inversion 3(q13q26) in the same patient. Ann G\u00e9n\u00e9t (Paris) 21:74?77","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR3","first-page":"77","volume":"17","author":"A Betz","year":"1974","unstructured":"Betz A, Turleau C, de Grouchy J (1974) Heterozygotie et homozygotie pour une inversion pericentrique du 3 humain. Ann G\u00e9n\u00e9t (Paris) 17:77?80","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR4","volume-title":"Repository of chromosomal variants and anomalies in man Tenth listing","author":"DS Borgaonkar","year":"1983","unstructured":"Borgaonkar DS, Shaffer R, Albright R, Reed WC, Jackson LG, Borgmann K, Simeral J (1983) Repository of chromosomal variants and anomalies in man Tenth listing. Wilmington Medical Center, Wilmington, Del; University of Delaware, Newark, Del; Thomas Jefferson University, Philadelphia, Pa"},{"key":"CR5","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1111\/j.1399-0004.1985.tb01224.x","volume":"27","author":"DF Callen","year":"1985","unstructured":"Callen DF, Woollatt E, Sutherland GR (1985) Paracentric inversions in man. Clin Genet 27:87?92","journal-title":"Clin Genet"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"341","DOI":"10.1002\/ajmg.1320240214","volume":"24","author":"M Campana","year":"1986","unstructured":"Campana M, Serra A, Neri G (1986) Role of chromosome aberrations in recurrent abortion: a study of 269 balanced translocations. Am J Hum Genet 24:341?356","journal-title":"Am J Hum Genet"},{"key":"CR7","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1007\/BF00321018","volume":"47","author":"N Canki","year":"1979","unstructured":"Canki N, Dutrillaux B (1979) Two cases of familial paracentric inversion in man associated with sex chromosome anomaly. 47,XXY, inv(5)(q21q32) and 45,X,inv(7)(q11.3q22.3). Hum Genet 47: 261?268","journal-title":"Hum Genet"},{"key":"CR8","doi-asserted-by":"crossref","first-page":"469","DOI":"10.1136\/jmg.19.6.469","volume":"19","author":"NJ Carpenter","year":"1982","unstructured":"Carpenter NJ, Say B, Barber ND (1982) A homozygote for pericentric inversion of chromosome 4. J Med Genet 19:469?471","journal-title":"J Med Genet"},{"key":"CR9","doi-asserted-by":"crossref","first-page":"345","DOI":"10.1002\/ajmg.1320050405","volume":"5","author":"BF Crandall","year":"1980","unstructured":"Crandall BF, Lebherz TB, Rubinstein L, Robertson RD, Sample WF, Sarti D, Howard J (1980) Chromosome findings in 2,500 second trimester amniocenteses. Am J Med Genet 5:345?356","journal-title":"Am J Med Genet"},{"key":"CR10","first-page":"746","volume":"26","author":"A Chapelle De la","year":"1974","unstructured":"De la Chapelle A, Schroder J, Stenstrand K, Fellman J, Herva R, Saarni M, Anttolainen I, Tallila I, Tervila L, Husa L, Tallqvist G, Robson EB, Cook PJL, Sanger R (1974) Pericentric inversions of human chromosomes 9 and 10. Am J Hum Genet 26:746?766","journal-title":"Am J Hum Genet"},{"key":"CR11","doi-asserted-by":"crossref","first-page":"451","DOI":"10.1136\/jmg.21.6.451","volume":"21","author":"G Porto Del","year":"1984","unstructured":"Del Porto G, D'Alessandro E, De Matteis C, D'Innocenzo R, Baldi M, Pachi A, Cappa F (1984) Familial paracentric inversion of chromosome 15 (q15q24). J Med Genet 21:451?453","journal-title":"J Med Genet"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"534","DOI":"10.1016\/S0022-3476(74)80673-6","volume":"84","author":"C Solar Del","year":"1974","unstructured":"Del Solar C, Uchida IA (1974) Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis. J Pediatr 84:534?538","journal-title":"J Pediatr"},{"key":"CR13","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1007\/BF00277632","volume":"49","author":"J Deroover","year":"1979","unstructured":"Deroover J, Fryns JP, Haegeman J, Van Den Berghe H (1979) Paracentric inversion in the short arm of chromosome 1. Hum Genet 49:117?121","journal-title":"Hum Genet"},{"key":"CR14","first-page":"41","volume":"27","author":"M Djalali","year":"1984","unstructured":"Djalali M, Steinbach P, Barbi G (1984) Familial paracentric inversion inv(3)(q21q25.1). Case report and review of the literature. Ann G\u00e9n\u00e9t (Paris) 27:41?44","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR15","doi-asserted-by":"crossref","first-page":"209","DOI":"10.1530\/jrf.0.0560209","volume":"56","author":"MJW Faed","year":"1979","unstructured":"Faed MJW, Robertson J, Lamont MA, MacIntosh W, Grieve J, Baxby K, James GB, Crowder AM (1979), A cytogenetic survey of men being investigated for subfertility. J Repord Fertil 56:209?216","journal-title":"J Repord Fertil"},{"key":"CR16","first-page":"163","volume":"22","author":"JP Fryns","year":"1979","unstructured":"Fryns JP, Van Den Berghe H (1979) Familial paracentric inversion of the short arm of chromosome 3. Ann G\u00e9n\u00e9t (Paris) 22:163?164","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR17","doi-asserted-by":"crossref","first-page":"413","DOI":"10.1007\/BF00291590","volume":"54","author":"JP Fryns","year":"1980","unstructured":"Fryns JP, Van Den Berghe H (1980) Paracentric inversion in man: personal experience and review of the literature. Hum Genet 54: 413?416","journal-title":"Hum Genet"},{"key":"CR18","doi-asserted-by":"crossref","first-page":"336","DOI":"10.1007\/BF00291558","volume":"65","author":"JP Fryns","year":"1984","unstructured":"Fryns JP, Kleczkowska A, Kubien E, Petit P Van Den Berghe H (1984) Cytogenetic survey in couples with recurrent fetal wastage. Hum Gene 65:336?354","journal-title":"Hum Gene"},{"key":"CR19","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1159\/000132006","volume":"37","author":"PS Gerald","year":"1984","unstructured":"Gerald PS, Grzeschik KH (1984) Report of the committee on the genetic constitution of chromosome 10, 11, and 12. Cytogenet Cell Genet 37:103?126","journal-title":"Cytogenet Cell Genet"},{"key":"CR20","first-page":"165","volume":"14","author":"RF Grell","year":"1971","unstructured":"Grell RF (1971) Distributive pairing in man? Ann G\u00e9n\u00e9t (Paris) 14: 165?171","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR21","unstructured":"Haapala K, Herva R, Leista J (1983) Paracentric inversion of chromosome 1 in a mother with unbalanced progeny. Abstracts of the 8th International Chromosome Conference, L\u00fcbeck, 1983"},{"key":"CR22","volume-title":"Practical genetic counselling","author":"PS Harper","year":"1984","unstructured":"Harper PS (1984) Practical genetic counselling, 2nd edn. Wright, Bristol","edition":"2nd edn"},{"key":"CR23","doi-asserted-by":"crossref","first-page":"140","DOI":"10.1136\/jmg.22.2.140","volume":"22","author":"HM Herr","year":"1985","unstructured":"Herr HM, Horton SJ, Scott CI Jr (1985) De novo paracentric inversion in an X chromosome. J Med Genet 22:140?142","journal-title":"J Med Genet"},{"key":"CR24","doi-asserted-by":"crossref","first-page":"1035","DOI":"10.1126\/science.472726","volume":"205","author":"SF Hoegerman","year":"1979","unstructured":"Hoegerman SF (1979) Chromosome 13 long arm interstitial deletion may result from maternal inverted, insertion. Science 205:1035?1036","journal-title":"Science"},{"key":"CR25","unstructured":"Hoo JJ, Lin CC (1983) Small paracentric inversion. Am J Hum Genet 35:134A"},{"key":"CR26","first-page":"113","volume":"62","author":"JJ Hoo","year":"1982","unstructured":"Hoo JJ, Lorenz R, Fischer A, Fuhrmann W (1982) Tiny interstitial duplication of proximal 7q in association with a maternal paracentric inversion. Hum Genet 62:113?116","journal-title":"Hum Genet"},{"key":"CR27","unstructured":"ISCN (1978) An international system for human cytogenetic nomenclature. Birth Defects 14, no 8"},{"key":"CR28","first-page":"105","volume":"23","author":"J Jaeken","year":"1980","unstructured":"Jaeken J, Fryns JP, Standaert L, De Cock P, Van Den Berghe H (1980) De novo paracentric invesion in a microcephalic boy: 46,XY,inv(14)(q13q24). Ann G\u00e9n\u00e9t (Paris) 23:105?107","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR29","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1007\/BF01873578","volume":"30","author":"R Kasai","year":"1985","unstructured":"Kasai R, Narahara K, Kikkawa K, Takahashi Y, Wakita Y, Kimura S, Kataoka N, Kimoto H (1985) Reproductive risk of paracentric inversion carriers: report of two unrelated cases with paracentric inversion of the long arm of chromoome 3. Jinrui Idengaku Zasshi 30:57?67","journal-title":"Jinrui Idengaku Zasshi"},{"key":"CR30","unstructured":"Kelly TE, Wyandt H, Kasprzak R, Ennis J, Willson K, Koch V, Schnatterly P (1979) Paracentric inversion: probable mechanism for an interstitial 3p deletion in a patient with multiple anomalies. Am J Hum Genet 31:100A"},{"key":"CR31","unstructured":"Knight LA, Lew S, Yiu M, Leverah J, Bannister V, Mann J (1983) Two cases of paracentric inversions detected prenatally. Am J Hum Genet 35:138A"},{"key":"CR32","first-page":"377","volume":"20","author":"RH Lindenbaum","year":"1981","unstructured":"Lindenbaum RH, Clarke G, Walker J (1981) Down's syndrome and paracentric inversion of 21q. Clin Genet 20:377","journal-title":"Clin Genet"},{"key":"CR33","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1136\/jmg.22.1.24","volume":"22","author":"RH Lindenbaum","year":"1985","unstructured":"Lindenbaum RH, Hulten M, McDermott A, Seabright M (1985) The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect? J Med Genet 22: 24?28","journal-title":"J Med Genet"},{"key":"CR34","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1136\/jmg.21.6.407","volume":"21","author":"K Madan","year":"1984","unstructured":"Madan K, Seabright M, Lindenbaum RH, Bobrow M (1984) Paracentric inversions in man. J Med Genet 21:407?412","journal-title":"J Med Genet"},{"key":"CR35","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1007\/BF00291594","volume":"73","author":"RH Martin","year":"1986","unstructured":"Martin RH (1986) Sperm chromosome analysis in a man heterozygous for a paracentric inversion of chromosome 7 (q11q22). Hum Genet 73:97?100","journal-title":"Hum Genet"},{"key":"CR36","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1002\/ajmg.1320200109","volume":"20","author":"NJ Martin","year":"1985","unstructured":"Martin NJ, Cartwright DW, Harvey PJ (1985) Duplication 5q (5q22 5q33): from an intrachromosomal insertion. Am J Med Genet 20: 57?62","journal-title":"Am J Med Genet"},{"key":"CR37","doi-asserted-by":"crossref","first-page":"310","DOI":"10.1159\/000132080","volume":"38","author":"P Martinez-Castro","year":"1984","unstructured":"Martinez-Castro P, Ramos MC, Rey JA, Benitez J, Sanchez Cascos A (1984) Homozygosity for a Robertsonian translocation(13q14q) in three offspring of heterozygous parents. Cytogenet Cell Genet 38:310?312","journal-title":"Cytogenet Cell Genet"},{"key":"CR38","first-page":"275","volume":"80","author":"N Morichon-Delvallez","year":"1985","unstructured":"Morichon-Delvallez N, Marchand F (1985a) A propos des inversions paracentriques: etude de deux nouvelles observations. Rev Fr Gynecol Obstet 80:275?277","journal-title":"Rev Fr Gynecol Obstet"},{"key":"CR39","first-page":"119","volume":"28","author":"N Morichon-Delvallez","year":"1985","unstructured":"Morichon-Delvallez N, Marchand F (1985b) Les inversions paracentriques chez l'homme. A propos de deux observations familiales. Ann G\u00e9n\u00e9t (Paris) 28:119?122","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR40","doi-asserted-by":"crossref","first-page":"126","DOI":"10.1007\/BF00272986","volume":"67","author":"EH Mules","year":"1984","unstructured":"Mules EH, Stamberg J (1984) Reproductive outcomes of paracentric inversion carriers: report of a liveborn dicentric recombinant and literature review. Hum Genet 67:126?131","journal-title":"Hum Genet"},{"key":"CR41","doi-asserted-by":"crossref","first-page":"231","DOI":"10.1136\/jmg.20.3.231","volume":"20","author":"E Orye","year":"1983","unstructured":"Orye E, Van Bever H (1983) Paracentric inversions: two new familial cases, inv(7)(q22q11) and inv(11)(q23q13). J Med Genet 20:231?232","journal-title":"J Med Genet"},{"key":"CR42","doi-asserted-by":"crossref","first-page":"102","DOI":"10.1111\/j.1399-0004.1982.tb01421.x","volume":"22","author":"MF Peters-Slough","year":"1982","unstructured":"Peters-Slough MF, Planteydt HT, Timmerman MJ, Vooren MJVD (1982) A familial paracentric inversion in the short arm of chromosome 3: a case report. Clin Genet 22:102?104","journal-title":"Clin Genet"},{"key":"CR43","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1136\/jmg.19.1.63","volume":"19","author":"AM Potter","year":"1982","unstructured":"Potter AM (1982) Variations in replication pattern and phenotype in two cases of X chromosome inversion. J Med Genet 19:63?67","journal-title":"J Med Genet"},{"key":"CR44","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1002\/pd.1970010108","volume":"1","author":"H Poulsen","year":"1981","unstructured":"Poulsen H, Mikkelsen M, Holmgren G (1981) Peri- and paracentric inversions in chromosome 12:prenatal diagnosis and family study. Prenat Diagn 1:35?42","journal-title":"Prenat Diagn"},{"key":"CR45","unstructured":"Remes GM, Grossman GL, Cousineau AJ, Higgins JV (1983) Dysmorphology associated with an apparently balanced de novo inversion of 2q. Am J Hum Genet 35:149A"},{"key":"CR46","doi-asserted-by":"crossref","first-page":"211","DOI":"10.1007\/BF00271575","volume":"52","author":"VM Riccardi","year":"1979","unstructured":"Riccardi VM, Homquist GP (1979) De novo 13q paracentric inversion in a boy with cleft palate and mental retardation. Hum Genet 52:211?215","journal-title":"Hum Genet"},{"key":"CR47","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1002\/pd.1970010113","volume":"1","author":"MAC Ridler","year":"1981","unstructured":"Ridler MAC, Sutton SD (1981) A case of paracentric inversion inv(7) (q11q22). Prenatal detection and counselling. Prenat Diagn 1:81?84","journal-title":"Prenat Diagn"},{"key":"CR48","first-page":"227","volume":"30","author":"SH Roberts","year":"1986","unstructured":"Roberts SH, Cowie VA, Rameshwari Singh K (1986) Intrachromosomal insertion of chromosome 13 in a family with psychosis and mental subnormality. J Ment Defic Res 30:227?232","journal-title":"J Ment Defic Res"},{"key":"CR49","doi-asserted-by":"crossref","first-page":"181","DOI":"10.1007\/BF00296437","volume":"61","author":"C Rockman-Greenberg","year":"1982","unstructured":"Rockman-Greenberg C, Ray M, Evans JA, Canning N, Hamerton JL (1982) Homozygous Robertsonian translocations in a fetus with 44 chromosomes. Hum Genet 61:181?184","journal-title":"Hum Genet"},{"key":"CR50","doi-asserted-by":"crossref","first-page":"629","DOI":"10.1002\/ajmg.1320140406","volume":"14","author":"DR Romain","year":"1983","unstructured":"Romain DR, Columbano-Green LM, Whyte S, Smythe RH, Parfitt RG, Gebbie OB, Chapman CJ (1983) Familial paracentric inversion of 1p. Am J Med Genet 14:629?634","journal-title":"Am J Med Genet"},{"key":"CR51","doi-asserted-by":"crossref","first-page":"270","DOI":"10.1007\/BF00284590","volume":"71","author":"M Schmid","year":"1985","unstructured":"Schmid M, Hofmann R, Kohler J, Jannek U (1985) Familial paracentric inversion inv(2)(q31q36). Hum Genet 71:270?272","journal-title":"Hum Genet"},{"key":"CR52","doi-asserted-by":"crossref","first-page":"971","DOI":"10.1016\/S0140-6736(71)90287-X","volume":"II","author":"M Seabright","year":"1971","unstructured":"Seabright M (1971) A rapid banding technique for human chromosomes. Lancet II:971?972","journal-title":"Lancet"},{"key":"CR53","first-page":"245","volume":"23","author":"F Shabtai","year":"1983","unstructured":"Shabtai F, Klar D, Zohar I, Halbrecht I (1983) Paracentric inversion in the long arm of chromosome X. Clin Genet 23:245?246","journal-title":"Clin Genet"},{"key":"CR54","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/BF00270393","volume":"31","author":"H Shimba","year":"1976","unstructured":"Shimba H, Ohtaki K, Tanabe K, Sofuni T (1976) Paracentric inversion of a human chromosome 7. Hum Genet 31:1?7","journal-title":"Hum Genet"},{"key":"CR55","doi-asserted-by":"crossref","first-page":"252","DOI":"10.1007\/BF00286612","volume":"66","author":"G Simoni","year":"1984","unstructured":"Simoni G, Brambati B, Danesino C, Terzoli GL, Romitti L, Rossella F, Fraccaro M (1984) Diagnostic application of first trimester trophoblast sampling in 100 pregnancies. Hum Genet 66:252?259","journal-title":"Hum Genet"},{"key":"CR56","doi-asserted-by":"crossref","first-page":"188","DOI":"10.1111\/j.1399-0004.1981.tb00694.x","volume":"19","author":"RP Singh","year":"1981","unstructured":"Singh RP (1981) Klinefelter's syndrome with a 47,XXY,inv(12) (q15q24) karyotype. Clin Genet 19:188?190","journal-title":"Clin Genet"},{"key":"CR57","doi-asserted-by":"crossref","first-page":"1027","DOI":"10.1126\/science.424728","volume":"203","author":"RS Sparkes","year":"1979","unstructured":"Sparkes RS, Muller H, Klisak I (1979) Retinoblastoma with 13q-chromosomal deletion associated with maternal paracentric inversion of 13q. Science 203:1027?1029","journal-title":"Science"},{"key":"CR58","doi-asserted-by":"crossref","first-page":"124","DOI":"10.1016\/S0015-0282(16)47190-6","volume":"40","author":"G Stetten","year":"1983","unstructured":"Stetten G, Rock JA (1983) A paracentric chromsomal inversion associated with repeated early pregnancy wastage. Fertil Steril 40: 124?126","journal-title":"Fertil Steril"},{"key":"CR59","unstructured":"Trunca C (1978) Paracentric inversions: a probable cause of fetal wastage. Am J Hum Genet 30:96A"},{"key":"CR60","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1007\/BF00285405","volume":"63","author":"E Valcarcel","year":"1983","unstructured":"Valcarcel E, Benitez J, Martinez P, Rey JA, Sanchez Cascos A (1983) Cytogenetic recombinants from a female carrying a paracentric inversion of the short arm of chromosome number 5. Hum Genet 63:78?81","journal-title":"Hum Genet"},{"key":"CR61","first-page":"301","volume":"35","author":"DL Dyke Van","year":"1982","unstructured":"Van Dyke DL, Weiss L, Roberson JR, Ramesh Babu V (1982) The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age. Am J Hum Genet 35:301?308","journal-title":"Am J Hum Genet"},{"key":"CR62","doi-asserted-by":"crossref","first-page":"181","DOI":"10.1002\/pd.1970040304","volume":"4","author":"LO Vejerslev","year":"1984","unstructured":"Vejerslev LO, Friedrich U (1984) Experiences with unexpected structural chromosome aberrations in prenatal diagnosis in a Danish series. Prenat Diagn 4:181?186","journal-title":"Prenat Diagn"},{"key":"CR63","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1007\/BF00272985","volume":"67","author":"PA Venter","year":"1984","unstructured":"Venter PA, Dawson B, Du Toit JL, Smith EL, Kritzinger N, Landman AS, Cronje AS, Op't Hof J (1984) A familial paracentric inversion: a short review of the current status. Hum Genet 67:121?125","journal-title":"Hum Genet"},{"key":"CR64","first-page":"16","volume-title":"Prenatal diagnosis","author":"M Verjaal","year":"1979","unstructured":"Verjaal M, Leschot NJ, Treffers PE, Der Weduwen JJ (1979) Unexpected chromosomal aberrations in prenatal diagnosis in ?older? women. In: Murken JD, Stengel-Rutkowski S, Schwinger E (eds) Prenatal diagnosis. Enke, Stuttgart, pp 16?18"},{"key":"CR65","first-page":"203","volume":"28","author":"DT Vine","year":"1976","unstructured":"Vine DT, Yarkoni S, Cohen MM (1976) Inversion homozygosity of chromosome no.9 in a highly inbred kindred. Am J Hum Genet 28:203?207","journal-title":"Am J Hum Genet"},{"key":"CR66","doi-asserted-by":"crossref","first-page":"132","DOI":"10.1159\/000130182","volume":"11","author":"J Wahrman","year":"1972","unstructured":"Wahrman J, Atidia J, Goitein R, Cohen T (1972) Pericentric inversions of chromosome 9 in two families. Cytogenetics 11:132?144","journal-title":"Cytogenetics"},{"key":"CR67","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1111\/j.1399-0004.1981.tb01048.x","volume":"20","author":"J Walker","year":"1981","unstructured":"Walker J, Lindenbaum RH (1981) A four-break rearrangement of chromosomes 7 and 13, with inversion and insertion, resulting in pure trisomy for the region 7q11.2 to 7q21.2. Clin Genet 20:363?402","journal-title":"Clin Genet"},{"key":"CR68","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1002\/pd.1970040706","volume":"4","author":"D Warburton","year":"1984","unstructured":"Warburton D (1984) Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis. Prenat Diagn. 4:69?80","journal-title":"Prenat Diagn"},{"key":"CR69","first-page":"143","volume":"1","author":"JL Watt","year":"1984","unstructured":"Watt JL, Couzin DA (1984) A case of interchromosomal effect? The Association of Clinical Cytogeneticists. Clin Cytogenet Bull 1:143","journal-title":"Clin Cytogenet Bull"},{"key":"CR70","first-page":"296","volume":"24","author":"M Wolf","year":"1981","unstructured":"Wolf M, Steinbach P (1981) DEL(1)(q25.2q31.2) and INV(1) (q31.2q44) in a severely retarded male with multiple anomalies, karyotype 46,XY,REA(1)(pterq25.2::q44q31.2::q44qter). Clin Genet 24:296","journal-title":"Clin Genet"},{"key":"CR71","first-page":"731","volume":"32","author":"HE Wyandt","year":"1980","unstructured":"Wyandt HE, Kasprzak R, Ennis J, Willson K, Koch V, Schnatterly P, Wilson W, Kelly TE (1980) Interstital 3q deletion in a child due to paternal paracentric inserted inversion. Am J Hum Genet 32: 731?735","journal-title":"Am J Hum Genet"},{"key":"CR72","first-page":"117","volume":"34","author":"CW Yu","year":"1976","unstructured":"Yu CW, Borgaonkar DS, Bolling DR (1976) Paracentric inversion in man. Hum Genet 34:117","journal-title":"Hum Genet"},{"key":"CR73","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1007\/BF00285963","volume":"67","author":"JJ Yunis","year":"1978","unstructured":"Yunis JJ, Sawyer JR, Ball DW (1978) The characterization of high-resolution G-banded chromosomes of man. Chromosoma 67: 293?307","journal-title":"Chromosoma"}],"container-title":["Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00591068.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00591068\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00591068","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,1,15]],"date-time":"2024-01-15T18:30:21Z","timestamp":1705343421000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00591068"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1987,2]]},"references-count":73,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1987,2]]}},"alternative-id":["BF00591068"],"URL":"https:\/\/doi.org\/10.1007\/bf00591068","relation":{},"ISSN":["0340-6717","1432-1203"],"issn-type":[{"value":"0340-6717","type":"print"},{"value":"1432-1203","type":"electronic"}],"subject":[],"published":{"date-parts":[[1987,2]]}}}