Publications
Export 2 results:
Filters: Keyword is Genetic Association Studies and Author is Gulec, Elif Yilmaz [Clear All Filters]
WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. Am J Hum Genet. 2018 ;102(1):27-43.
. De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease. Hum Genet. 2016 ;135(12):1399-1409.
.