Identification of Novel SHOX Target Genes in the Developing Limb Using a Transgenic Mouse Model

Author:

Beiser Katja U.,Glaser Anne,Kleinschmidt Kerstin,Scholl Isabell,Röth Ralph,Li Li,Gretz Norbert,Mechtersheimer Gunhild,Karperien Marcel,Marchini Antonio,Richter Wiltrud,Rappold Gudrun A.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference44 articles.

1. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome;E Rao;Nat Genet,1997

2. Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis;DJ Shears;Nat Genet,1998

3. Phenotypes Associated with SHOX Deficiency;JL Ross;J Clin Endocrinol Metab,2001

4. Rappold GA, Ross JL, Blaschke RJ, Blum W (2002) Understanding SHOX deficiency and its role in growth disorders. A reference guide. Oxfordshire, UK: TMG Healthcare Communications Ltd.

5. Pseudodominant inheritance of Langer mesomelic dysplasia caused by a SHOX homeobox missense mutation;DJ Shears;Am J Med Genet,2002

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