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

Research output: Contribution to journalArticlepeer-review

71 Scopus citations

Fingerprint

Dive into the research topics of 'The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: Contrasting children with Leri-Weill dyschondrosteosis and turner syndrome'. Together they form a unique fingerprint.

Medicine & Life Sciences