J Müller, G Cobet, G Laske, B Degen, C Grauel, K Lehmann
{"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}
引用次数: 0
Abstract
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.
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