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Journal of Neurology|January 18, 2005
LGI1 gene mutation screening in sporadic partial epilepsy with auditory featuresE Flex, A Pizzuti, C Di Bonaventura, et al.Human Genetics|April 1, 1990
Genetic differences in cystic fibrosis patients with and without pancreatic insufficiency. An Italian collaborative studyM Ferrari, M Antonelli, F Bellini, et al.Human Genetics|April 6, 1999
Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibilityS Semprini, F Capon, S Bovolenta, et al.Clinical Genetics|January 1, 1997
Two mosaic-YY males carrying asymmetric Y chromosomesL Zelante, B Dallapiccola, S Calvano, et al.European Review for Medical and Pharmacological Sciences|February 24, 2006
The polymorphism of multi-drug resistance 1 gene (MDR1) does not influence the pharmacokinetics of dexamethasone loaded into autologous erythrocytes of patients with inflammatory bowel diseaseV Annese, A Latiano, L Rossi, et al.Pediatric Radiology|January 1, 1992
Radiographic findings in Wiedemann-Rautenstrauch syndromeM G Obregon, G L Bergami, A Giannotti, et al.Annales De Genetique|January 1, 1992
Molecular studies of a translocated (X;22) DiGeorge patient using somatic cell hybridizationP Couillin, J Zucman, E Le Guern, et al.European Journal of Human Genetics : EJHG|September 26, 2001
Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26M Mangino, E Flex, F Capon, et al.Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1990
Regional distribution of cystic fibrosis linked DNA haplotypes in Italy, a collaborative studyP Gasparini, N Cappello, B Dallapiccola, et al.Circulation|December 6, 2001
Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrenceM C Digilio, B Casey, A Toscano, et al.Pageof 34