{"title":"新生儿迪乔治综合征——诊断挑战","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":"{\"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}","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}