Showing results (31-40 of 62) with videos related to
Sort By:
Pageof 7
Cytogenetic and Genome Research|October 30, 2009
Characterization of a 5.8-Mb interstitial deletion of chromosome 3p in a girl with 46,XX,inv(7)dn karyotype and phenotypic abnormalitiesC Morales, I Mademont-Soler, L Armengol, et al.Human Genetics|October 28, 1997
Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardationM Milà, A Sànchez, C Badenas, et al.American Journal of Medical Genetics. Part A|April 14, 2007
Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsyL Rodriguez-Revenga, I Madrigal, L S Alkhalidi, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|August 2, 2012
Benefits of oral Polypodium Leucotomos extract in MM high-risk patientsP Aguilera, C Carrera, J A Puig-Butille, et al.Oncogene|September 26, 2001
A melanoma-associated germline mutation in exon 1beta inactivates p14ARFH Rizos, S Puig, C Badenas, et al.The British Journal of Dermatology|September 18, 2008
Dermoscopic features of melanomas associated with MC1R variants in Spanish CDKN2A mutation carriersF Cuéllar, S Puig, I Kolm, et al.Kidney International|July 20, 1999
Seven novel mutations of the PKD2 gene in families with autosomal dominant polycystic kidney diseaseR Torra, M Viribay, D Tellería, et al.Genetic Testing|March 6, 2004
Incidence of fragile X in 5,000 consecutive newborn malesM Rifé, C Badenas, J Mallolas, et al.Clinical Genetics|March 23, 2004
Cryptic chromosomal rearrangement screening in 30 patients with mental retardation and dysmorphic featuresL Rodriguez-Revenga, C Badenas, A Sánchez, 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.Pageof 7