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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Vydáno v:Zdr Varst
Hlavní autoři: HOVNIK, Tinka, ŠMIGOC SCHWEIGER, Darja, KOTNIK, Primož, KOVAČ, Jernej, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina
Médium: Artigo
Jazyk:Inglês
Vydáno: De Gruyter Open 2015
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Original Scientific Article
On-line přístup: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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