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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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Bibliografiset tiedot
Päätekijät: Poskitt, E. M. E., Rayner, P. H. W.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1974
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1648860/
https://ncbi.nlm.nih.gov/pubmed/4361890
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