Autosomal dominant inheritance of Weaver syndrome.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 9152841.
- Also identified by PMC identifier 1050951.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Most report of Weaver syndrome have been sporadic cases and the genetic basis of the syndrome is uncertain. This report of an affected father and daughter provides evidence for autosomal dominant inheritance.
Medical subject headings
- Genes, Dominant
- Genetic Diseases, Inborn
- Growth Disorders