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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Zdr Varst
Egile Nagusiak: HOVNIK, Tinka, ŠMIGOC SCHWEIGER, Darja, KOTNIK, Primož, KOVAČ, Jernej, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: De Gruyter Open 2015
Gaiak:
Original Scientific Article
Sarrera elektronikoa: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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