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Brachydactyly, Type A1, B
National Institutes of Health
Autosomal dominant inheritance
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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
American journal of medical genetics. Part A
Corpus ID: 27267297
The identification of chromosomal breakpoints in association with human abnormal phenotypes can enable elucidation of gene…
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