Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansion

Autor: Horsnell, Katherine a, Ali, Manir b, Malik, Saghira c, Wilson, Louise d, Hall, Christine e, Debeer, Philippe f, ⁎, Crow, Yanick c
Zdroj: In European Journal of Medical Genetics 2006 49(5):396-401
Databáze: ScienceDirect