{"title":"DiGeorge Syndrome In A Newborn - A Diagnostic Challenge","authors":"V. Carvalho","doi":"10.24966/ncp-878x/100061","DOIUrl":null,"url":null,"abstract":"DiGeorge syndrome is mainly caused by microdeletion of chromosome 22 (22q11.2) and is characterized by a broad phenotypic spectrum.","PeriodicalId":93307,"journal":{"name":"Journal of clinical pediatrics and neonatology","volume":"45 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of clinical pediatrics and neonatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24966/ncp-878x/100061","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
DiGeorge syndrome is mainly caused by microdeletion of chromosome 22 (22q11.2) and is characterized by a broad phenotypic spectrum.
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