Showing results (1-10 of 74) with videos related to
Sort By:
Pageof 8
Molecular Genetics and Metabolism|February 13, 2001
Genes responsible for nonspecific mental retardationS Castellví-Bel, M MilàJournal of Medical Genetics|April 1, 1996
Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 geneM Milà, S Castellví-Bel, A Sánchez, et al.Medicina Clinica|May 10, 1997
[Molecular analysis of the IT15 gene in 79 Spanish families with Huntington's disease: diagnostic confirmation and presymptomatic diagnosis]A Sánchez, M Milà, S Castellví-Bel, et al.American Journal of Medical Genetics|February 15, 2001
Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21C Badenas, S Castellví-Bel, V Volpini, et al.Human Genetics|October 1, 1996
A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansionM Milà, S Castellví-Bel, R Giné, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1997
Maternal transmission in sporadic Huntington's diseaseA Sánchez, M Milà, S Castellví-Bel, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1996
Huntington's disease: confirmation of diagnosis and presymptomatic testing in Spanish families by genetic analysisA Sánchez, S Castellví-Bel, M Milà, et al.Menopause (New York, N.Y.)|March 21, 2001
Implications of the FMR1 gene in menopause: study of 147 Spanish womenJ Mallolas, M Duran, A Sánchez, et al.Molecular and Cellular Probes|May 9, 2000
Rare variants in the promoter of the fragile X syndrome gene (FMR1)M Milà, S Castellví-Bel, A Sánchez, et al.Journal of Medical Genetics|August 1, 1994
Chemiluminescent detection of blotted PCR products (CB-PCR) of two CAG dynamic mutations (Huntington's disease and spinocerebellar ataxia type 1)S Castellví-Bel, T Matilla, M I Banchs, et al.Pageof 8