J Müller, G Cobet, G Laske, B Degen, C Grauel, K Lehmann
{"title":"[智障男孩的部分单体或胎儿酒精性胚胎病?]。","authors":"J Müller, G Cobet, G Laske, B Degen, C Grauel, K Lehmann","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>A male newborn showed dysmorphisms combined with a complex cerebral malformation and a growth retardation. Alcohol damage in utero was suspected to be the cause. A deletion 21q (mosaic) was found in the karyotype.</p>","PeriodicalId":19624,"journal":{"name":"Padiatrie und Grenzgebiete","volume":"31 5","pages":"313-9"},"PeriodicalIF":0.0000,"publicationDate":"1993-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Partial monosomy 21 or fetal alcohol embryopathy in a retarded boy?].\",\"authors\":\"J Müller, G Cobet, G Laske, B Degen, C Grauel, K Lehmann\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A male newborn showed dysmorphisms combined with a complex cerebral malformation and a growth retardation. Alcohol damage in utero was suspected to be the cause. A deletion 21q (mosaic) was found in the karyotype.</p>\",\"PeriodicalId\":19624,\"journal\":{\"name\":\"Padiatrie und Grenzgebiete\",\"volume\":\"31 5\",\"pages\":\"313-9\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1993-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Padiatrie und Grenzgebiete\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Padiatrie und Grenzgebiete","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Partial monosomy 21 or fetal alcohol embryopathy in a retarded boy?].
A male newborn showed dysmorphisms combined with a complex cerebral malformation and a growth retardation. Alcohol damage in utero was suspected to be the cause. A deletion 21q (mosaic) was found in the karyotype.