Condition: Robinow Syndrome


rs786200925 in WNT5A gene and Robinow Syndrome PMID 19918918 2010 WNT5A mutations in patients with autosomal dominant Robinow syndrome.

PMID 24716670 2015 De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype.