Orden según fecha de publicación:
Identification of a frameshift mutation in Osterix in a patient with recessive osteogenesis imperfecta
Lapunzina P, Aglan M, Temtamy S, Caparrós-Martín JA, Valencia M, Letón R, Martínez-Glez V, Elhossini R, Amr K, Vilaboa N, Ruiz-Perez VL. Am J Hum Genet. 2010 Jul 9;87(1):110-4. Epub 2010 Jun 24
Identification of 31 novel mutations in the F8 gene in Spanish hemophilia A patients: structural analysis of 20 missense mutations suggests new intermolecular binding sites
Venceslá A, Corral-Rodríguez MA, Baena M, Cornet M, Domènech M, Baiget M, Fuentes-Prior P, Tizzano EF. Blood. 2008 Apr 1;111(7):3468-78. Epub 2008 Jan 9
