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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
  • Debeer, P
  • Bacchelli, C
  • Scambler, P J
  • De Smet, L
  • Fryns, J-P
  • Goodman, F R
Type
Published Article
Journal
Journal of Medical Genetics
Publisher
BMJ
Publication Date
Nov 01, 2002
Volume
39
Issue
11
Pages
852–856
Identifiers
PMID: 12414828
Source
Medline
License
Unknown
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