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American Journal of Medical Genetics|May 20, 1999
Single-strand conformation polymorphism analysis in the FMR1 geneS Castellví-Bel, A Sánchez, C Badenas, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|August 23, 2006
Genetic studies in variegate porphyria in Spain. Identification of gene mutations and family study for carrier detectionM Lecha, C Badenas, S Puig, et al.Neurology|October 13, 2010
Motor and mental dysfunction in mother-daughter transmitted FXTASL Rodriguez-Revenga, J Pagonabarraga, B Gómez-Anson, et al.Molecular Human Reproduction|August 24, 2004
Analysis of CGG variation through 642 meioses in Fragile X familiesM Rifé, C Badenas, Ll Quintó, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 29, 2000
Increased prevalence of polycystic kidney disease type 2 among elderly polycystic patientsR Torra, C Badenas, L Pérez-Oller, et al.Gene|June 23, 2015
Deregulation of key signaling pathways involved in oocyte maturation in FMR1 premutation carriers with Fragile X-associated primary ovarian insufficiencyM I Alvarez-Mora, L Rodriguez-Revenga, I Madrigal, et al.Human Genetics|October 1, 1996
YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndromeM Nadal, M Milà, M Pritchard, et al.Human Genetics|October 1, 1994
Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome familiesM Milà, H Kruyer, G Glover, et al.Fertility and Sterility|October 3, 1998
Prevalence of Y chromosome microdeletions in oligospermic and azoospermic candidates for intracytoplasmic sperm injectionR Oliva, E Margarit, J L Ballescá, et al.Revista Espanola De Medicina Nuclear|September 29, 2004
[Adrenal cortex scintigraphy with and without dexamethasone suppression in the study of primary aldosteronism]M Milà López, J Castell-Conesa, P Pifarré Montaner, et al.Pageof 7