Paternal uniparental disomy of chromosome 1 is an uniparental disomy of paternal origin that most likely does not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only father is a carrier.
Comprehensive, easy-to-understand information about this condition
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ring chromosome 1
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mosaic trisomy 1
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silver-Russell syndrome due to maternal uniparental disomy of chromosome 11
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maternal uniparental disomy of chromosome 1
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maternal uniparental disomy of chromosome X
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