Showing results (1-10 of 63) with videos related to
Sort By:
Pageof 7
Revista De Neurologia|November 26, 2002
[Fragile X syndrome: premature ovarian failure. Preimplantation and preconception genetic diagnosis]M Milà, J MallolasMolecular Genetics and Metabolism|February 13, 2001
Genes responsible for nonspecific mental retardationS Castellví-Bel, M MilàAmerican Journal of Medical Genetics. Part A|December 31, 2003
Immunohistochemical FMRP studies in a full mutated female fetusM Rifé, A Nadal, M Milà, et al.Pediatric Cardiology|July 2, 2005
Elastin mutation screening in a group of patients affected by vascular abnormalitiesL Rodriguez-Revenga, C Badenas, A Carrió, et al.Clinical Genetics|November 15, 2002
SCA8 in the Spanish population including one homozygous patientB Tazón, C Badenas, L Jiménez, et al.Revista De Neurologia|October 25, 2006
[Genetic mental retardation]L Rodríguez-Revenga Bodi, I Madrigal-Bajo, M Milà-RacasensJournal of Intellectual Disability Research : JIDR|February 12, 2008
Deletion of the OPHN1 gene detected by aCGHI Madrigal, L Rodríguez-Revenga, C Badenas, et al.Journal of Inherited Metabolic Disease|June 16, 2007
Complete deletion of ornithine transcarbamylase gene confirmed by CGH array of X chromosomeJ A Arranz, I Madrigal, E Riudor, et al.Anales De Pediatria (Barcelona, Spain : 2003)|November 1, 2003
[FMRP immunodetection on hair roots: application to the diagnosis of fragile X syndrome]M Rifé Soler, A Sánchez Díaz, F Ramos, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 4, 1999
Influence of the ACE gene polymorphism in the progression of renal failure in autosomal dominant polycystic kidney diseaseL Pérez-Oller, R Torra, C Badenas, et al.Pageof 7