Genetic analysis of familial isolated growth hormone deficiency type I.

Nuclear DNA from individuals belonging to nine different families in which two sibs were affected with isolated growth hormone deficiency type I were studied by restriction endonuclease analysis. By using 32P-labeled human growth hormone or the homologous human chorionic somatomammotropin complement...

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Pubblicato in:	J Clin Invest
Autori principali:	Phillips, J A, Parks, J S, Hjelle, B L, Herd, J E, Plotnick, L P, Migeon, C J, Seeburg, P H
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	American Society for Clinical Investigation 1982
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC370249/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6286724/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI110640
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