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Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13.

Authors
Type
Published Article
Journal
Journal of Medical Genetics
1468-6244
Publisher
BMJ
Publication Date
Volume
39
Issue
11
Pages
852–856
Identifiers
PMID: 12414828
Source
Medline

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