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Medicina Clinica|May 5, 1990
[Genetic analysis of Friedreich's ataxia using polymorphic DNA markers]F Palau, J J Vílchez, M Beneyto, et al.Human Mutation|July 29, 1999
Identification of three novel mutations in the MYO7A geneJ M Cuevas, C Espinós, J M Millán, et al.Journal of Medical Genetics|June 4, 1998
Linkage analysis in Usher syndrome type I (USH1) families from SpainC Espinós, C Nájera, J M Millán, et al.Human Mutation|February 5, 2000
Identification of two rare variants (G-->A at nucleotide 721; C-->T at nucleotide 5200) in the rhodopsin gene. Mutations in brief no. 187. OnlineM J Trujillo, J M Millán, C Nájera, et al.Human Genetics|July 1, 1995
Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish familiesM Bayés, D Valverde, S Balcells, et al.Prenatal Diagnosis|October 17, 2006
Gene duplications in 21-hydroxylase deficiency: the importance of accurate molecular diagnosis in carrier detection and prenatal diagnosisB Ezquieta, M Beneyto, R Muñoz-Pacheco, et al.Molecular and Cellular Probes|December 9, 1998
Detection of a novel Cys628STOP mutation of the myosin VIIA gene in Usher syndrome type IbJ M Cuevas, C Espinós, J M Millán, et al.Ophthalmic Genetics|March 1, 1996
Clinical and genetic aspects of two Spanish families with autosomal dominant retinitis pigmentosa (ADRP)C Vilela, M Beneyto, R Bosch, et al.American Journal of Human Genetics|June 13, 2001
A common ancestral origin of the frequent and widespread 2299delG USH2A mutationB Dreyer, L Tranebjaerg, V Brox, et al.Human Genetics|June 1, 1997
Putative association of a mutant ROM1 allele with retinitis pigmentosaA Martínez-Mir, C Vilela, M Bayés, et al.Pageof 4