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- W2079983872 abstract "Holt-Oram syndrome is an autosomal dominant disorder with variable expression. From a review of published pedigree data and of a family reported here, we have found that penetrance is 100 % if appropriate studies, including wrist radiographs, are performed. There does not appear to be a significant maternal effect on the severity of expression in affected offspring." @default.
- W2079983872 created "2016-06-24" @default.
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- W2079983872 date "2008-04-23" @default.
- W2079983872 modified "2023-10-01" @default.
- W2079983872 title "Holt-Oram syndrome: penetrance of the gene and lack of maternal effect" @default.
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- W2079983872 doi "https://doi.org/10.1111/j.1399-0004.1982.tb00743.x" @default.
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