Original paper
Brachydactyly Type B: Linkage to Chromosome 9q22 and Evidence for Genetic Heterogeneity
Volume: 64, Issue: 2, Pages: 578 - 585
Published: Feb 1, 1999
Abstract
Brachydactyly type B (BDB), an autosomal dominant disorder, is the most severe of the brachydactylies and is characterized by hypoplasia or absence of the terminal portions of the index to little fingers, usually with absence of the nails. The thumbs may be of normal length but are often flattened and occasionally are bifid. The feet are similarly but less severely affected. We have performed a genomewide linkage analysis of three families with...
Paper Details
Title
Brachydactyly Type B: Linkage to Chromosome 9q22 and Evidence for Genetic Heterogeneity
Published Date
Feb 1, 1999
Volume
64
Issue
2
Pages
578 - 585
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