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Isolated growth hormone deficiency: Two families with autosomal dominant inheritance

Two families, each with a father and a son affected by isolated growth hormone deficiency, are described. The inheritance in these cases seems to be due to an autosomal dominant gene. Isolated growth hormone deficiency appears to be a heterogeneous condition.

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מידע ביבליוגרפי
Main Authors: Poskitt, E. M. E., Rayner, P. H. W.
פורמט: Artigo
שפה:Inglês
יצא לאור: 1974
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC1648860/
https://ncbi.nlm.nih.gov/pubmed/4361890
תגים: הוספת תג
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