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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Detalhes bibliográficos
Publicado no:J Clin Invest
Main Authors: Phillips, J A, Parks, J S, Hjelle, B L, Herd, J E, Plotnick, L P, Migeon, C J, Seeburg, P H
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 1982
Assuntos:
Research Article
Acesso em linha: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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