Associated Papers
A novel variant in the ROR2 gene underlying brachydactyly type B: a case report.
Shao J et al.
Bmc Pediatrics, 2022
Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations.
Aglan M et al.
American Journal of Medical Genetics. Part A, 2015
Clinical and molecular characterization of two adults with autosomal recessive Robinow syndrome.
Tufan F et al.
American Journal of Medical Genetics. Part A, 2005
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