دورية أكاديمية

Novel variant in NSDHL gene associated with CHILD syndrome and syndactyly- a case report

التفاصيل البيبلوغرافية
العنوان: Novel variant in NSDHL gene associated with CHILD syndrome and syndactyly- a case report
المؤلفون: Hettiarachchi, D.Aff1, Panchal, Hetalkumar, Lai, P. S., Dissanayake, V. H. W.
المصدر: BMC Medical Genetics. 21(1)
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:14712350
DOI:10.1186/s12881-020-01094-y