M. Faed, V. Marrian, J. Robertson, E. Robson, P. Cook
{"title":"遗传性5号染色体周中心倒位:有新生儿死亡史的家族和“cri du chat”综合征1例。","authors":"M. Faed, V. Marrian, J. Robertson, E. Robson, P. Cook","doi":"10.1097/00006254-197306000-00018","DOIUrl":null,"url":null,"abstract":"Only a few families have been recorded in which an inherited pericentric inversion has been shown to give rise to a chromosome with a duplication-deletion in a child with congenital malformations. Thi","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"11 5 1","pages":"400-11"},"PeriodicalIF":0.0000,"publicationDate":"1973-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1097/00006254-197306000-00018","citationCount":"27","resultStr":"{\"title\":\"Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the \\\"cri du chat\\\" syndrome.\",\"authors\":\"M. Faed, V. Marrian, J. Robertson, E. Robson, P. Cook\",\"doi\":\"10.1097/00006254-197306000-00018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Only a few families have been recorded in which an inherited pericentric inversion has been shown to give rise to a chromosome with a duplication-deletion in a child with congenital malformations. Thi\",\"PeriodicalId\":78202,\"journal\":{\"name\":\"Cytogenetics\",\"volume\":\"11 5 1\",\"pages\":\"400-11\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1973-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1097/00006254-197306000-00018\",\"citationCount\":\"27\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cytogenetics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1097/00006254-197306000-00018\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cytogenetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/00006254-197306000-00018","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome.
Only a few families have been recorded in which an inherited pericentric inversion has been shown to give rise to a chromosome with a duplication-deletion in a child with congenital malformations. Thi
求助内容：
应助结果提醒方式：
京公网安备 11010802042870号
