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American Journal of Human Genetics|March 1, 1994
Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twinsH Kruyer, M Milà, G Glover, et al.Journal 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|July 30, 1999
[Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome]M Milà, A Carrió, A Sánchez, et al.Molecular Genetics and Metabolism|June 5, 1999
Biochemical phenotype and its relationship with genotype in hyperphenylalaninemia heterozygotesJ Mallolas, M Milà, N Lambruschini, et al.Revista Espanola De Medicina Nuclear E Imagen Molecular|January 23, 2023
[Nuclear Cardiology in the COVID-19 pandemic]M Milà López, A Jiménez Heffernan, E Sánchez de Mora, 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.Journal of the Neurological Sciences|July 20, 2002
Intranuclear inclusions, neuronal loss and CAG mosaicism in two patients with Machado-Joseph diseaseE Muñoz, M J Rey, M Milà, 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.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.Pageof 7