Cytogenetic and Molecular Genetic Characterization of Children with Short Stature

BACKGROUND: The deficiency of SHOX gene (short stature homeobox-containing gene) has been recognized as the most frequent monogenetic cause of short stature. SHOX gene has been associated with short stature in Turner syndrome and Leri Weill dyschondrosteosis as well with non-syndromic idiopathic sho...

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Detalles Bibliográficos
Autores principales: HOVNIK, Tinka, ŠMIGOC SCHWEIGER, Darja, KOTNIK, Primož, KOVAČ, Jernej, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter Open 2015
Materias:
Original Scientific Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820174/
https://www.ncbi.nlm.nih.gov/pubmed/27646915
http://dx.doi.org/10.1515/sjph-2015-0015

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820174/
https://www.ncbi.nlm.nih.gov/pubmed/27646915
http://dx.doi.org/10.1515/sjph-2015-0015

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