Below are the most recent publications written about "Short Stature Homeobox Protein" by people in Profiles.
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Benito-Sanz S, Belinchon-Mart?nez A, Aza-Carmona M, de la Torre C, Huber C, Gonz?lez-Casado I, Ross JL, Thomas NS, Zinn AR, Cormier-Daire V, Heath KE. Identification of 15 novel partial SHOX deletions and 13 partial duplications, and a review of the literature reveals intron 3 to be a hotspot region. J Hum Genet. 2017 Feb; 62(2):229-234.
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Benito-Sanz S, Barroso E, Heine-Su?er D, Hisado-Oliva A, Romanelli V, Rosell J, Aragones A, Caimari M, Argente J, Ross JL, Zinn AR, Gracia R, Lapunzina P, Campos-Barros A, Heath KE. Clinical and molecular evaluation of SHOX/PAR1 duplications in Leri-Weill dyschondrosteosis (LWD) and idiopathic short stature (ISS). J Clin Endocrinol Metab. 2011 Feb; 96(2):E404-12.
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Shah BC, Moran ES, Zinn AR, Pappas JG. Effect of growth hormone therapy on severe short stature and skeletal deformities in a patient with combined Turner syndrome and Langer mesomelic dysplasia. J Clin Endocrinol Metab. 2009 Dec; 94(12):5028-33.
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Campos-Barros A, Benito-Sanz S, Ross JL, Zinn AR, Heath KE. Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD). Am J Med Genet A. 2007 May 01; 143A(9):933-8.
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Zinn AR, Ramos P, Ross JL. A second recombination hotspot associated with SHOX deletions. Am J Hum Genet. 2006 Mar; 78(3):523-5.
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Ross JL, Kowal K, Quigley CA, Blum WF, Cutler GB, Crowe B, Hovanes K, Elder FF, Zinn AR. The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome. J Pediatr. 2005 Oct; 147(4):499-507.
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Ross JL, Bellus G, Scott CI, Abboudi J, Grigelioniene G, Zinn AR. Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasia. Am J Med Genet A. 2003 Jan 01; 116A(1):61-5.
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Zinn AR, Wei F, Zhang L, Elder FF, Scott CI, Marttila P, Ross JL. Complete SHOX deficiency causes Langer mesomelic dysplasia. Am J Med Genet. 2002 Jun 15; 110(2):158-63.
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Ross JL, Scott C, Marttila P, Kowal K, Nass A, Papenhausen P, Abboudi J, Osterman L, Kushner H, Carter P, Ezaki M, Elder F, Wei F, Chen H, Zinn AR. Phenotypes Associated with SHOX Deficiency. J Clin Endocrinol Metab. 2001 Dec; 86(12):5674-80.