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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Detalles Bibliográficos

Publicado en:	J Clin Invest
Autores principales:	Phillips, J A, Parks, J S, Hjelle, B L, Herd, J E, Plotnick, L P, Migeon, C J, Seeburg, P H
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	American Society for Clinical Investigation 1982
Materias:	Research Article
Acceso en línea:	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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