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pubmed-article:16014698pubmed:abstractTextBrachydactyly type A2 (OMIM 112600) is characterised by hypoplasia/aplasia of the second middle phalanx of the index finger and sometimes the little finger. BDA2 was first described by Mohr and Wriedt in a large Danish/Norwegian kindred and mutations in BMPR1B were recently demonstrated in two affected families.lld:pubmed
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pubmed-article:16014698pubmed:articleTitleA mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2.lld:pubmed
pubmed-article:16014698pubmed:affiliationWilhelm Johannsen Centre for Functional Genome Research, Department of Medical Biochemistry and Genetics, University of Copenhagen, Denmark. klaus@medgen.ku.dklld:pubmed
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