Associated Papers
Clinical and molecular characterization of four patients with Robinow syndrome from different families.
Rai A et al.
American Journal of Medical Genetics. Part A, 2021
Characterization of the Robinow syndrome skeletal phenotype, bone micro-architecture, and genotype-phenotype correlations with the osteosclerotic form.
Shayota BJ et al.
American Journal of Medical Genetics. Part A, 2020
DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome.
White J et al.
American Journal of Human Genetics, 2015
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