Sequence Variants in <i>MEGF8</i> and <i>GJA1</i> Underlying Syndactyly.

导出 OA

翻译打印收藏纠错

作者： Muhammad,Bilal ^[1] ; Tobias B,Haack ^[2] ; Rebecca,Buchert ^[2] ; Susana,Peralta ^[2] ; Najum,Uddin ^[3] ; Raja Hussain,Ali ^[4] ; Khurram,Liaqat ^[5] ; Wasim,Ahmad ^[1]

作者单位： Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan. ^[1] Institute for Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany. ^[2] National Centre for Bioinformatics, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan. ^[3] Department of Hematology/Oncology, Boston Children's Hospital, Boston, Massachusetts, USA. ^[4] Center for Statistical Genetics, Gertrude H. Sergievsky Center, and the Department of Neurology, Columbia University Medical Center, New York, New York, USA. ^[5]

关键词 GJA1 MEGF8 Novel variants Syndactyly Whole-exome sequencing

DOI 10.1159/000528651

PMID 37323198

发布时间 2023-12-02

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交