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Paper Details

Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome.
Am J Med Genet A
15
2021
DVL1, DVL3, FZD2, NXN, ROR2, RS, Robinow syndrome, Robinow-associated genes, WNT5A, pathogenic genomic variants, skeletal dysplasia
Author NameAffiliation
Zeynep Coban AkdemirBaylor College of Medicine
Shalini N JhangianiBaylor College of Medicine
Donna M MuznyBaylor College of Medicine
Donna M MuznyBaylor College of Medicine
Richard A GibbsBaylor College of Medicine
Richard A GibbsBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiTexas Children's Hospital
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiTexas Children's Hospital
James R LupskiBaylor College of Medicine
Vernon R SuttonBaylor College of Medicine
Vernon R SuttonTexas Children's Hospital
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