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High incidence of SHOX anomalies in individuals with short stature

OBJECTIVE: To study the SHOX gene and the PAR1 region in individuals with short stature. METHODS: The study involved 56 cases of dyschondrosteosis and 84 cases of idiopathic short stature (ISS). The study was designed to determine the following: the prevalence of SHOX anomalies in ISS; the frequency...

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Hlavní autoři: Huber, C, Rosilio, M, Munnich, A, Cormier‐Daire, V
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Group 2006
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2564573/
https://ncbi.nlm.nih.gov/pubmed/16597678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.040998
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