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...

Popoln opis

Bibliografske podrobnosti

izdano v:	J Clin Invest
Principais autores:	Phillips, J A, Parks, J S, Hjelle, B L, Herd, J E, Plotnick, L P, Migeon, C J, Seeburg, P H
Format:	Artigo
Jezik:	Inglês
Izdano:	American Society for Clinical Investigation 1982
Teme:	Research Article
Online dostop:	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
Oznake:	Označite Brez oznak, prvi označite!