The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: Contrasting children with Leri-Weill dyschondrosteosis and turner syndrome

Judith L. Ross, Karen Kowal, Charmian A. Quigley, Werner F. Blum, Gordon B. Cutler, Brenda Crowe, Karine Hovanes, Frederick F. Elder, Andrew R. Zinn

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