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 |
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Zdroj: | In European Journal of Medical Genetics 2006 49(5):396-401 |
Databáze: | ScienceDirect |
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