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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Detaylı Bibliyografya
Yayımlandı:J Clin Invest
Asıl Yazarlar: Phillips, J A, Parks, J S, Hjelle, B L, Herd, J E, Plotnick, L P, Migeon, C J, Seeburg, P H
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Clinical Investigation 1982
Konular:
Research Article
Online Erişim: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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