Biallelic loss ‐of‐function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome

American Journal of Medical Genetics Part A,Volume 176, Issue 4, Page 1030-1036, April 2018.

Source: American Journal of Medical Genetics Part A - March 25, 2018 Category: Genetics & Stem Cells Source Type: research