Refreshing results…
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome
Download from www.nature.comA second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region
Download from academic.oup.comGenetic features of retinitis pigmentosa in Turkey
UploadA large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?
Download from www.ncbi.nlm.nih.govMissing publications? Search for publications with a matching author name.