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Molecular basis for familial isolated growth hormone deficiency.

Nuclear DNA from four individuals with familial isolated growth hormone (somatotropin) deficiency (IGHD) type A was studied by restriction endonuclease analysis. By using 32P-labeled human growth hormone (hGH) cDNA sequences as a probe, patterns seen after various digestions indicated that these ind...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Phillips, J A, Hjelle, B L, Seeburg, P H, Zachmann, M
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 1981
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC349041/
https://ncbi.nlm.nih.gov/pubmed/6273867
Tagiau: Ychwanegu Tag
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