Limb skeletal malformations – What the HOX is going on?
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference59 articles.
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4. Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13;Debeer;J. Med. Genet.,2002
5. Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families;Goodman;Am. J. Hum. Genet.,1998
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