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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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| Publicado no: | Zdr Varst |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
De Gruyter Open
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4820174/ https://ncbi.nlm.nih.gov/pubmed/27646915 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1515/sjph-2015-0015 |
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