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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Bibliografische gegevens
Gepubliceerd in:Zdr Varst
Hoofdauteurs: HOVNIK, Tinka, ŠMIGOC SCHWEIGER, Darja, KOTNIK, Primož, KOVAČ, Jernej, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: De Gruyter Open 2015
Onderwerpen:
Original Scientific Article
Online toegang: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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