AMOTL1 De Novo Mutation Associated with Orofacial Clefting, Ocular Colobomas, an Atrial Septal Defect and Digital Anomalies: A Case Report and Review of the Literature
{"title":"AMOTL1 De Novo Mutation Associated with Orofacial Clefting, Ocular Colobomas, an Atrial Septal Defect and Digital Anomalies: A Case Report and Review of the Literature","authors":"","doi":"10.29011/2575-825x.100223","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":8302,"journal":{"name":"Archives of pediatrics","volume":"20 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of pediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29011/2575-825x.100223","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}