Isolated growth hormone deficiency. Two families with autosomal dominant inheritance
- PMID: 4361890
- PMCID: PMC1648860
- DOI: 10.1136/adc.49.1.55
Isolated growth hormone deficiency. Two families with autosomal dominant inheritance
Abstract
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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