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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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| Pubblicato in: | Zdr Varst |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
De Gruyter Open
2015
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| Soggetti: | |
| Accesso online: | 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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