Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
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.
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.
Clinical and Experimental Dermatology|May 9, 2008
Childhood-onset mild cutaneous porphyria with compound heterozygotic mutations in the uroporphyrinogen decarboxylase geneE Remenyik, M Lecha, C Badenas, et al.
American Journal of Human Genetics|March 7, 1998
Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosidesX Estivill, N Govea, E Barceló, et al.
The British Journal of Dermatology|May 8, 2013
Distribution of MC1R variants among melanoma subtypes: p.R163Q is associated with lentigo maligna melanoma in a Mediterranean populationJ A Puig-Butillé, C Carrera, R Kumar, et al.
The British Journal of Dermatology|September 3, 2017
Acquired erythropoietic uroporphyria secondary to myelodysplastic syndrome with chromosome 3 alterations: a case reportS Podlipnik, F Guijarro, A Combalia, et al.
Reproductive Biomedicine Online|August 31, 2010
Fragile X syndrome prenatal diagnosis: parental attitudes and reproductive responsesM Xunclà, C Badenas, M Domínguez, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 27, 2020
Dermoscopy comparative approach for early diagnosis in familial melanoma: influence of MC1R genotypeC Longo, V Barquet, E Hernandez, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 26, 2022
Synchronous primary cutaneous melanomas: a descriptive study of their clinical features, histology, genetic background of the patients and clinical outcomesA Antúnez-Lay, S Podlipnik, C Carrera, et al.
Pageof 7