Associated Papers
A novel variant in the ROR2 gene underlying brachydactyly type B: a case report.
Shao J et al.
Bmc Pediatrics, 2022
A homozygous ROR2 variant in a family with atypical Robinow syndrome and tetramelic transverse deficiency of autopods.
Malik S et al.
American Journal of Medical Genetics. Part A, 2022
Mutation screening in candidate genes in four Chinese brachydactyly families.
Dong S et al.
Annals of Clinical and Laboratory Science, 2015
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