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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Опубликовано в::	J Clin Invest
Главные авторы:	Phillips, J A, Parks, J S, Hjelle, B L, Herd, J E, Plotnick, L P, Migeon, C J, Seeburg, P H
Формат:	Artigo
Язык:	Inglês
Опубликовано:	American Society for Clinical Investigation 1982
Предметы:	Research Article
Online-ссылка:	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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