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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Sparad:
Bibliografiska uppgifter
I publikationen:Zdr Varst
Huvudupphovsmän: HOVNIK, Tinka, ŠMIGOC SCHWEIGER, Darja, KOTNIK, Primož, KOVAČ, Jernej, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina
Materialtyp: Artigo
Språk:Inglês
Publicerad: De Gruyter Open 2015
Ämnen:
Original Scientific Article
Länkar: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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