Condition: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1


rs869025215 in DVL3 gene and ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 PMID 26924530 2016 DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome.

rs387906663 in WNT5A gene and ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 PMID 19918918 2010 WNT5A mutations in patients with autosomal dominant Robinow syndrome.