{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T12:54:10Z","timestamp":1761742450836},"reference-count":65,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[1983,12,1]],"date-time":"1983-12-01T00:00:00Z","timestamp":439084800000},"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":[[1983,12]]},"DOI":"10.1007\/bf00286654","type":"journal-article","created":{"date-parts":[[2004,10,5]],"date-time":"2004-10-05T08:37:16Z","timestamp":1096965436000},"page":"155-164","source":"Crossref","is-referenced-by-count":51,"title":["The genetic significance of accessory bisatellited marker chromosomes"],"prefix":"10.1007","volume":"65","author":[{"given":"P.","family":"Steinbach","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Djalali","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Hansmann","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Kattner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Meisel-Stosiek","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H. -D.","family":"Probeck","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Schmidt","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Wolf","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"338","DOI":"10.1111\/j.1399-0004.1971.tb00294.x","volume":"2","author":"J Aitken","year":"1971","unstructured":"Aitken J, Brunton M, Jacobs PA, Price WH, McColl K (1971) Chromosome studies on male patients at a mental subnormality hospital. Clin Genet 2: 338?346","journal-title":"Clin Genet"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1159\/000130060","volume":"8","author":"S Armendares","year":"1969","unstructured":"Armendares S, Buentello L, Cuevas-Sosa A, Cant\u00fa-Garza JM (1969) Familial extra-centric bisatellited chromosome. Cytogenetics 8: 177?186","journal-title":"Cytogenetics"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1007\/BF00291576","volume":"54","author":"HD Bartsch","year":"1980","unstructured":"Bartsch HD, de Azevedo Moreira LM, R\u00f6hrborn G, Claussen U, Gebauer HJ (1980) Possible origin of a small bisatellited additional chromosome. Hum Genet 54: 319?322","journal-title":"Hum Genet"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1136\/jmg.15.2.136","volume":"15","author":"R Bernstein","year":"1978","unstructured":"Bernstein R, Hakim C, Hardwick B, Nurse GT (1978) Significance of detection of extra metacentric microchromosome in amniotic cell culture. J Med Genet 15: 136?142","journal-title":"J Med Genet"},{"key":"CR5","first-page":"207","volume":"19","author":"S Borgaonkar","year":"1971","unstructured":"Borgaonkar S, Schimke RN, Thomas H (1971) Report of five unrelated patients with a small metacentric, extra chromosome or fragment. J Genet Hum 19: 207?222","journal-title":"J Genet Hum"},{"key":"CR6","first-page":"474","volume":"63","author":"WH Borges","year":"1963","unstructured":"Borges WH, Wald N (1963) A diminutive satellited chromosome in a father and in one of two true hermaphrodite progeny. Midwest Soc Pediat Res 63: 474?475","journal-title":"Midwest Soc Pediat Res"},{"key":"CR7","first-page":"59","volume":"44","author":"K Br\u00f8ndum-Nielsen","year":"1978","unstructured":"Br\u00f8ndum-Nielsen K, Dyggve H, Friedrich U, Hobolth N, Lyngbye T, Mikkelsen M (1978) Small metacentric nonsatellited extra chromosome. Report of five mentally retarded individuals and review of literature. Contribution to further delineation of a new syndrome. Hum Genet 44: 59?69","journal-title":"Hum Genet"},{"key":"CR8","doi-asserted-by":"crossref","first-page":"287","DOI":"10.1007\/BF00273515","volume":"53","author":"a Calabro","year":"1980","unstructured":"Calabro a, Lungarotti MS, Dallapiccola B (1980) A comment on the paper: Recurrence of Down syndrome associated with microchromosome. By Ramos C, Rivera L, Benitez J, Tejedor E, and Sanchez-Cascos A. Hum Genet 53: 287?288","journal-title":"Hum Genet"},{"key":"CR9","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1002\/ajmg.1320050113","volume":"5","author":"R Carmi","year":"1980","unstructured":"Carmi R, Abeliovich D, Bar-Ziv J, Karplus M, Cohen MM (1980) Malformation syndrome associated with small extra chromosome. Am J Med Genet 5: 101?107","journal-title":"Am J Med Genet"},{"key":"CR10","first-page":"97","volume":"23","author":"H Chen","year":"1980","unstructured":"Chen H, Harris J (1980) Prenatal diagnosis in the presence of an extra small chromosome in amniotic cell culture. Ann G\u00e9n\u00e9t (Paris) 23: 97?99","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR11","doi-asserted-by":"crossref","first-page":"62","DOI":"10.1016\/S0022-3476(72)80454-2","volume":"80","author":"BF Crandall","year":"1972","unstructured":"Crandall BF, Carrel RE, Sparkes RS (1972) Chromosome findings in 700 children referred to a psychiatric clinic. J Pediatr 80: 62?68","journal-title":"J Pediatr"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1136\/jmg.16.3.227","volume":"16","author":"A Daniel","year":"1979","unstructured":"Daniel A (1979) Normal phenotype and partial trisomy for the G positive region of chromosome 21. J Med Genet 16: 227?235","journal-title":"J Med Genet"},{"key":"CR13","unstructured":"De Falco JE, Willey AM (1978) Three cases of partial tetrasomy 15. Am J Hum Genet 30: 17A"},{"key":"CR14","first-page":"45","volume":"18","author":"AC Gutierrez De","year":"1975","unstructured":"De Gutierrez AC, Salamanca F, Lisker R, Segovia A (1975) Supernumerary bisatellited chromosome in a family ascertained through a patient with Sturge-Weber syndrome. Ann G\u00e9n\u00e9t (Paris) 18: 45?49","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR15","first-page":"197","volume":"23","author":"R Dzarlieva","year":"1975","unstructured":"Dzarlieva R, Efinski D, ?opova M (1975) Genetic prognosis and counseling in the presence of extra small chromosomes. J G\u00e9n\u00e9t Hum 23: 197?206","journal-title":"J G\u00e9n\u00e9t Hum"},{"key":"CR16","doi-asserted-by":"crossref","first-page":"536","DOI":"10.1136\/jmg.8.4.536","volume":"8","author":"AJ Ebbin","year":"1971","unstructured":"Ebbin AJ, Wilson MG, Towner JW, Forsman I (1971) An inherited 1:G translocation. J Med Genet 8: 536?539","journal-title":"J Med Genet"},{"key":"CR17","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1111\/j.1469-1809.1962.tb01312.x","volume":"26","author":"JR Ellis","year":"1962","unstructured":"Ellis JR, Marshall R, Penrose LS (1962) An aberrant small acrocentric chromosome. Ann Hum Genet 26: 77?83","journal-title":"Ann Hum Genet"},{"key":"CR18","doi-asserted-by":"crossref","first-page":"191","DOI":"10.1111\/j.1399-0004.1979.tb00990.x","volume":"16","author":"MJW Faed","year":"1979","unstructured":"Faed MJW, Robertson J, Field AS, Mellon JP (1979) A chromosome survey of a hospital for the mentally subnormal. Clin Genet 16: 191?204","journal-title":"Clin Genet"},{"key":"CR19","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1111\/j.1399-0004.1979.tb00983.x","volume":"16","author":"K Fleischer-Michaelsen","year":"1979","unstructured":"Fleischer-Michaelsen K, Lundsteen C, Juul Hansen F (1979) Prader-Willi syndrome and chromosomal mosaicism 46,XX\/46,XY, +mar in two cases. Clin Genet 16: 147?150","journal-title":"Clin Genet"},{"key":"CR20","doi-asserted-by":"crossref","first-page":"371","DOI":"10.1159\/000153075","volume":"29","author":"K Fried","year":"1979","unstructured":"Fried K, Rosenblatt M (1979) A familial extra small marker autosome in persons with normal phenotype. Hum Hered 29: 371?373","journal-title":"Hum Hered"},{"key":"CR21","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1111\/j.1399-0004.1974.tb00626.x","volume":"6","author":"U Friedrich","year":"1974","unstructured":"Friedrich U, Nielsen J (1974) Bisatellited extra small metacentric chromosome in newborns. Clin Genet 6: 23?31","journal-title":"Clin Genet"},{"key":"CR22","doi-asserted-by":"crossref","first-page":"111","DOI":"10.1007\/BF00396487","volume":"43","author":"E Grace","year":"1978","unstructured":"Grace E, Sills J (1978) The occurrence of a ring 18, an accessory bisatellited fragment, and trisomy 21 within one sibship. Hum Genet 43: 111?114","journal-title":"Hum Genet"},{"key":"CR23","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1111\/j.1399-0004.1981.tb00666.x","volume":"19","author":"H Haas-Andela","year":"1981","unstructured":"Haas-Andela H, Hansen S, Foerster W, Fuhrmann W (1981) Familial additional chromosomal fragment ascertained in amniotic cell culture. Clin Genet 19: 46?50","journal-title":"Clin Genet"},{"key":"CR24","first-page":"393","volume":"8","author":"I Henrichs","year":"1982","unstructured":"Henrichs I, Wolf M, Steinbach P, Teller WM (1982) Diskrete klinische Auff\u00e4lligkeiten bei kleinem \u00fcberz\u00e4hligem ringf\u00f6rmigem Chromosomenfragment mit aktiver NOR. Wissenschaftliche Information der Milupa AG 8: 393?397","journal-title":"Wissenschaftliche Information der Milupa AG"},{"key":"CR25","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1159\/000130089","volume":"9","author":"H Hoehn","year":"1970","unstructured":"Hoehn H, Reinwein H, Engel W (1970) Genetic studies on a minute centric fragment transmitted through three generations. Cytogenetics 9: 186?198","journal-title":"Cytogenetics"},{"key":"CR26","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1007\/BF00281003","volume":"25","author":"JJ Hoo","year":"1974","unstructured":"Hoo JJ, Forster C, Kindermann I, Zabel B, Hansen S (1974) Supernumerary small ring chromosome. Humangenetik 25: 17?28","journal-title":"Humangenetik"},{"key":"CR27","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1002\/ajmg.1320050403","volume":"5","author":"JJ Hoo","year":"1980","unstructured":"Hoo JJ, Drummond M, Parslow I, Chambers D (1980) The ring nature of a tiny supernumerary chromosome fragment. Am J Med Genet 5: 331?337","journal-title":"Am J Med Genet"},{"key":"CR28","doi-asserted-by":"crossref","first-page":"347","DOI":"10.1093\/oxfordjournals.jhered.a109272","volume":"70","author":"PN Howard-Peebles","year":"1979","unstructured":"Howard-Peebles PN (1979) A familial bisatellited extra metacentric microchromosome in man. J Hered 70: 347?348","journal-title":"J Hered"},{"key":"CR29","doi-asserted-by":"crossref","first-page":"167","DOI":"10.1002\/ajmg.1320020208","volume":"2","author":"G Kohn","year":"1978","unstructured":"Kohn G, Shaham M, Ornoy A, Beyth Y, Cohen MM (1978) Small marker chromosome mosaicism confirmed in two cases ascertained prenatally. Am J Med Genet 2: 167?173","journal-title":"Am J Med Genet"},{"key":"CR30","doi-asserted-by":"crossref","first-page":"130","DOI":"10.1111\/j.1399-0004.1978.tb02117.x","volume":"14","author":"E Lieber","year":"1978","unstructured":"Lieber E, Shah P, Hack M (1978) Hazards of amniocentesis: An unidentifiable fragment. Clin Genet 14: 130?132","journal-title":"Clin Genet"},{"key":"CR31","doi-asserted-by":"crossref","first-page":"365","DOI":"10.1007\/BF00291584","volume":"54","author":"MG Mattei","year":"1980","unstructured":"Mattei MG, Mattei JF, Vidal I, Giraud F (1980) Advantages of silver staining in seven rearrangements of acrocentric chromosomes, excluding Robertsonian translocations. Hum Genet 54: 365?370","journal-title":"Hum Genet"},{"key":"CR32","first-page":"62","volume":"18","author":"D Mukerjee","year":"1966","unstructured":"Mukerjee D, Burdette WJ (1966) A familial minute isochromosome. Am J Hum Genet 18: 62?69","journal-title":"Am J Hum Genet"},{"key":"CR33","doi-asserted-by":"crossref","first-page":"1333","DOI":"10.5694\/j.1326-5377.1972.tb92924.x","volume":"2","author":"MT Mulcahy","year":"1972","unstructured":"Mulcahy MT, Jenkyn J (1972) Results of 538 chromosome studies on patients referred for cytogenetic analysis. Med J Aust 2: 1333?1338","journal-title":"Med J Aust"},{"key":"CR34","doi-asserted-by":"crossref","first-page":"253","DOI":"10.1111\/j.1399-0004.1980.tb00882.x","volume":"18","author":"G Neri","year":"1980","unstructured":"Neri G, Cagiano Malvezzi D, Serra A, Bova R, Pelino A, Maugiatti L (1980) Properties and significance of a small chromosome in amniotic fluid cells. Clin Genet 18: 253?256","journal-title":"Clin Genet"},{"key":"CR35","doi-asserted-by":"crossref","first-page":"226","DOI":"10.1111\/j.1399-0004.1972.tb04271.x","volume":"3","author":"MS Newton","year":"1972","unstructured":"Newton MS, Cunningham C, Jacobs PA, Price WH, Fraser IA (1972) Chromosome survey of a hospital for the mentally subnormal. Part 2: Autosome abnormalities. Clin Genet 3: 226?248","journal-title":"Clin Genet"},{"key":"CR36","doi-asserted-by":"crossref","first-page":"221","DOI":"10.1111\/j.1601-5223.1975.tb01036.x","volume":"81","author":"J Nielsen","year":"1975","unstructured":"Nielsen J, Rasmussen K (1975) Extra marker chromosome in newborn children. Hereditas 81: 221?224","journal-title":"Hereditas"},{"key":"CR37","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1007\/BF00295236","volume":"19","author":"J Nielsen","year":"1973","unstructured":"Nielsen J, Hreidarsson AB (1973) Father and daughter with presumptive isochromosome. Satellites-short arms D or G. Humangenetik 19: 271?274","journal-title":"Humangenetik"},{"key":"CR38","doi-asserted-by":"crossref","first-page":"184","DOI":"10.1111\/j.1399-0004.1977.tb01297.x","volume":"11","author":"K Ogata","year":"1977","unstructured":"Ogata K, Iinuma K, Kamimura K, Morinaga R, Kato J (1977) A case report of a presumptive +i(18p) associated with serum IgA deficiency. Clin Genet 11: 184?188","journal-title":"Clin Genet"},{"key":"CR39","first-page":"124","volume":"10","author":"RA Pfeiffer","year":"1967","unstructured":"Pfeiffer RA, Diekmann L, Buchner T (1967) Familial occurrence of a small metacentric extra chromosome with satellites on both ends. Ann G\u00e9n\u00e9t (Paris) 10: 124?130","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR40","first-page":"159","volume":"20","author":"MM Power","year":"1977","unstructured":"Power MM, Barry RG, Cannon DE, Materson JG (1977) Familial partial trisomy 15. Ann G\u00e9n\u00e9t (Paris) 20: 159?165","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR41","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1111\/j.1399-0004.1976.tb02268.x","volume":"9","author":"WH Price","year":"1976","unstructured":"Price WH, Brunton M, Buckton K, Jacobs PA (1976) Chromosome survey ofnew patients admitted to the four maximum security hospitals in the United Kingdom. Clin Genet 9: 389?398","journal-title":"Clin Genet"},{"key":"CR42","first-page":"117","volume":"24","author":"F Prieto","year":"1981","unstructured":"Prieto F, Badia L, Ribes C, Medina VH (1981) Trisomie 21 par translocation 21\/21 chez deux fils d'une mere avec un microchromosome surnumeraire. Ann G\u00e9n\u00e9t (Paris) 24: 117?119","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR43","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1007\/BF00277682","volume":"49","author":"C Ramos","year":"1979","unstructured":"Ramos C, Rivera L, Benitez J, Tejedor E, Sanchez-Cascos A (1979) Recurrence of Down syndrome associated with microchromosome. Hum Genet 49: 7?10","journal-title":"Hum Genet"},{"key":"CR44","first-page":"114","volume":"11","author":"N Ricci","year":"1968","unstructured":"Ricci N, Ventimiglia B, Preto G (1968) Transmission d'un petit chromosome surnum\u00e9raire dans une famille avec deux cas de trisomie 21. Ann G\u00e9n\u00e9t (Paris) 11: 114?116","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR45","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1136\/jmg.7.2.148","volume":"7","author":"MAC Ridler","year":"1970","unstructured":"Ridler MAC, Berg JM, Pendrey J, Salda\u00f1a P, Timothy JAD (1970) Familial occurrence of a small, supernumerary metacentric chromosome in phenotypically normal women. J Med Genet 7: 148?152","journal-title":"J Med Genet"},{"key":"CR46","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1136\/jmg.16.1.69","volume":"16","author":"M Rocci","year":"1979","unstructured":"Rocci M, Stormi M, Archidiacono N, Filippi G (1979) Extra small metacentric chromosome identified as i(18p). J Med Genet 16: 69?73","journal-title":"J Med Genet"},{"key":"CR47","doi-asserted-by":"crossref","first-page":"243","DOI":"10.1136\/jmg.2.4.243","volume":"2","author":"RA Rohde","year":"1965","unstructured":"Rohde RA (1965) A masculinizing syndrome associated with a doubly unsatellited extra chromosome. J Med Genet 2: 243?245","journal-title":"J Med Genet"},{"key":"CR48","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1111\/j.1399-0004.1979.tb00989.x","volume":"16","author":"DR Romain","year":"1979","unstructured":"Romain DR, Columbano-Green L, Smythe RH, Dukes PCM (1979) Discovery of an inherited bisatellited microchromosome in amniotic cell culture. Clin Genet 16: 183?190","journal-title":"Clin Genet"},{"key":"CR49","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1038\/hdy.1980.5","volume":"44","author":"AM Salmasi","year":"1980","unstructured":"Salmasi AM, Malcolm S, Elliot T, Williamson R, Ferguson-Smith MA (1980) Nucleolus-organiser regions in familial extra metacentric human chromosomes. Heredity 44: 63?68","journal-title":"Heredity"},{"key":"CR50","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1007\/BF00282012","volume":"57","author":"A Schinzel","year":"1981","unstructured":"Schinzel A, Schmid W, Fraccaro M, Tiepolo L, Zuffardi O, Opitz JM, Lindsten J, Zetterqvist P, Enell H, Baccichetti C, Tenconi R, Pagon RA (1981) The ?cat eye syndrome?: Dicentric small marker chromosome probably derived from a no. 22 (tetrasomy 22pter?q11) associated with characteristic phenotype. Report of 11 patients and delineation of the clinical picture. Hum Genet 57: 148?158","journal-title":"Hum Genet"},{"key":"CR51","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/BF00390430","volume":"36","author":"PR Schreck","year":"1977","unstructured":"Schreck PR, Breg WR, Erlanger BF, Miller OJ (1977) Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15. Hum Genet 36: 1?12","journal-title":"Hum Genet"},{"key":"CR52","doi-asserted-by":"crossref","first-page":"61","DOI":"10.1136\/jmg.18.1.61","volume":"18","author":"A Smith","year":"1981","unstructured":"Smith A, Fraser IS, Shearman RP (1981) A 13-year-old girl with karyotype 47,XX,+i(22)(q11). J Med Genet 18: 61?64","journal-title":"J Med Genet"},{"key":"CR53","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1159\/000129858","volume":"4","author":"KD Smith","year":"1965","unstructured":"Smith KD, Steinberger E, Steinberger A, Perloff W (1965) A familial centric chromosome fragment. Cytogenetics 4: 219?226","journal-title":"Cytogenetics"},{"key":"CR54","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1111\/j.1399-0004.1977.tb00942.x","volume":"12","author":"D Soudek","year":"1977","unstructured":"Soudek D, Sroka H (1977) C-bands in seven cases of accessory small chromosomes. Clin Genet 12: 285?289","journal-title":"Clin Genet"},{"key":"CR55","first-page":"101","volume":"2","author":"D Soudek","year":"1973","unstructured":"Soudek D, McCreary BD, Laraya P, Dill FJ (1973) Two kinships with accessory bisatellited chromosomes. Ann G\u00e9n\u00e9t (Paris) 2: 101?107","journal-title":"Ann G\u00e9n\u00e9t (Paris)"},{"key":"CR56","doi-asserted-by":"crossref","first-page":"295","DOI":"10.1136\/jmg.13.4.295","volume":"13","author":"RM Speed","year":"1976","unstructured":"Speed RM, Johnston AW, Evans HJ (1976) Chromosome survey of total population of mentally subnormal in north-east of Scotland. J Med Genet 13: 295?306","journal-title":"J Med Genet"},{"key":"CR57","doi-asserted-by":"crossref","first-page":"402","DOI":"10.1007\/BF00292376","volume":"64","author":"P Steinbach","year":"1983","unstructured":"Steinbach P, Djalali M (1983) Ineffectivity of accessory bisatellited marker chromosomes in inducing meiotic nondisjunction. Hum Genet 64: 402?403","journal-title":"Hum Genet"},{"key":"CR58","doi-asserted-by":"crossref","first-page":"357","DOI":"10.1007\/BF00281684","volume":"57","author":"G Stetten","year":"1981","unstructured":"Stetten G, Sroka-Zaczek B, Corson VL (1981) Prenatal detection of an accessory chromosome identified as an inversion duplication (15). Hum Genet 57: 357?359","journal-title":"Hum Genet"},{"key":"CR59","first-page":"327","volume":"111","author":"RE Stevenson","year":"1966","unstructured":"Stevenson RE, Patterson RB, Goodman HO (1966) Possible autosomal isochromosome in a malformed child. Am J Dis Child 111: 327?332","journal-title":"Am J Dis Child"},{"key":"CR60","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1136\/jmg.7.4.407","volume":"7","author":"I ?ubrt","year":"1970","unstructured":"?ubrt I, Prchlikova H (1970) An extra chromosomal centric fragment in an infant with stigmata of Down's syndrome. J Med Genet 7: 407?409","journal-title":"J Med Genet"},{"key":"CR61","doi-asserted-by":"crossref","first-page":"231","DOI":"10.1007\/BF00295286","volume":"34","author":"GR Sutherland","year":"1976","unstructured":"Sutherland GR, Murch AR, Gardiner AJ, Carter RF, Wiseman C (1976) Cytogenetic survey of a hospital for the mentally retarded. Hum Genet 34: 231?245","journal-title":"Hum Genet"},{"key":"CR62","doi-asserted-by":"crossref","first-page":"275","DOI":"10.1111\/j.1399-0004.1977.tb00941.x","volume":"12","author":"KE Toomey","year":"1977","unstructured":"Toomey KE, Mohandas T, Leisti J, Szalay G, Kaback MM (1977) Further delineation of the supernumerary chromosome in the cat-eye syndrome. Clin Genet 12: 275?284","journal-title":"Clin Genet"},{"key":"CR63","doi-asserted-by":"crossref","first-page":"438","DOI":"10.1016\/S0022-3476(69)80202-7","volume":"74","author":"S Walzer","year":"1969","unstructured":"Walzer S, Breau G, Gerald PS (1969) A chromosome survey of 2400 normal newborn infants. J Pediatr 74: 438?448","journal-title":"J Pediatr"},{"key":"CR64","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1007\/BF00399391","volume":"50","author":"L Wisniewski","year":"1979","unstructured":"Wisniewski L, Hassold T, Heffelfinger J, Higgins JV (1979) Cytogenetic and clinical studies in five cases of inv dup(15). Hum Genet 50: 259?270","journal-title":"Hum Genet"},{"key":"CR65","doi-asserted-by":"crossref","first-page":"42","DOI":"10.1111\/j.1399-0004.1980.tb01363.x","volume":"18","author":"L Wisniewski","year":"1980","unstructured":"Wisniewski L, Witt ME, Ginsberg-Fellner F, Wilner J, Desnick RJ (1980) Prader-Willi syndrome and a bisatellited derivative of chromosome 15. Clin Genet 18: 42?47","journal-title":"Clin Genet"}],"container-title":["Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00286654.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00286654\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00286654","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,1,14]],"date-time":"2024-01-14T14:21:15Z","timestamp":1705242075000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00286654"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1983,12]]},"references-count":65,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1983,12]]}},"alternative-id":["BF00286654"],"URL":"https:\/\/doi.org\/10.1007\/bf00286654","relation":{},"ISSN":["0340-6717","1432-1203"],"issn-type":[{"value":"0340-6717","type":"print"},{"value":"1432-1203","type":"electronic"}],"subject":[],"published":{"date-parts":[[1983,12]]}}}