Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13.
J Med Genet. 2002 Nov;39(11):852-6. doi: 10.1136/jmg.39.11.852.
J Med Genet. 2002.
PMID: 12414828
Free PMC article.
No abstract available.