Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13
Open Access
- 1 November 2002
- journal article
- letter
- Published by BMJ in Journal of Medical Genetics
- Vol. 39 (11) , 852-856
- https://doi.org/10.1136/jmg.39.11.852
Abstract
No abstract availableKeywords
This publication has 0 references indexed in Scilit: