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International Journal of Molecular Medicine|April 5, 2005
Polymorphisms in the promoter regions of FAS and FASL genes as candidate genetic factors conferring susceptibility to endometriosisR M Fernández, J A Noval, J C García-Lozano, et al.
Clinical Genetics|October 1, 1994
Molecular and clinical analyses of cystic fibrosis in the south of SpainS Borrego, T Casals, J Dapena, et al.
Journal of Medical Genetics|April 5, 2005
Ancestral RET haplotype associated with Hirschsprung's disease shows linkage disequilibrium breakpoint at -1249R M Fernandez, G Boru, A Peciña, et al.
Neurologia|October 22, 2022
Barcelona scale for buccophonatory apraxia: Quantitative assessment toolN Montagut, S Borrego-Écija, J Herrero, et al.
Scientific Reports|October 9, 2019
LncRNA LUCAT1 as a novel prognostic biomarker for patients with papillary thyroid cancerB Luzón-Toro, R M Fernández, J M Martos-Martínez, et al.
Annals of Human Genetics|December 2, 2008
A novel point variant in NTRK3, R645C, suggests a role of this gene in the pathogenesis of Hirschsprung diseaseR M Fernández, A Sánchez-Mejías, M D Mena, et al.
Annals of Human Genetics|May 31, 2008
Linkage validation of RP25 Using the 10K genechip array and further refinement of the locus by new linked familiesI Barragán, M M Abd El-Aziz, S Borrego, et al.
Journal of Medical Genetics|February 9, 1999
High prevalence of the C634Y mutation in the RET proto-oncogene in MEN 2A families in SpainB Sánchez, M Robledo, J Biarnes, et al.
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