Brachydactyly, Type A1, B

Known as: BDA1B 
 
National Institutes of Health

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Autosomal dominant inheritanceClinodactylyGenetic Heterogeneity

Broader (1)

Brachydactyly

Papers overview

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2015
2015
Co-segregation of Freiberg's infraction with a familial translocation t(5;7)(p13.3;p22.2) ascertained by a child with cri du chat syndrome and brachydactyly type A1B.
The identification of chromosomal breakpoints in association with human abnormal phenotypes can enable elucidation of gene… (More)
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