학술논문

A novel truncating variant in the FGD1 gene associated with Aarskog–Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly
Document Type
Article
Source
In: American Journal of Medical Genetics, Part A. (American Journal of Medical Genetics, Part A, October 2021, 185(10):3161-3166)
Subject
Language
English
ISSN
15524833
15524825