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Human Genetics|September 1, 1989
Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two south European populationsX Estivill, P Gasparini, G Novelli, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndromeF Amati, E Conti, A Novelli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Anatomic patterns of conotruncal defects associated with deletion 22q11B Marino, M C Digilio, A Toscano, et al.
Clinical Genetics|June 1, 1995
Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variantA Grifa, M R Piemontese, S Melchionda, et al.
Archives of Disease in Childhood|December 1, 1982
Early iron overload in beta-thalassaemia major: when to start chelation therapy?S Fargion, M T Taddei, V Gabutti, et al.
The Journal of Investigative Dermatology|May 12, 2001
Fine mapping of the PSORS4 psoriasis susceptibility region on chromosome 1q21F Capon, S Semprini, S Chimenti, et al.
European Journal of Human Genetics : EJHG|May 30, 2003
A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1M Mangino, D C Salpietro, D Zuccarello, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 23, 2003
Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4AF Brancati, E M Valente, N P Davies, et al.
The Journal of Investigative Dermatology|January 14, 1999
Searching for psoriasis susceptibility genes in Italy: genome scan and evidence for a new locus on chromosome 1F Capon, G Novelli, S Semprini, et al.
Applied and Environmental Microbiology|October 18, 2015
Genomic Diversity of Phages Infecting Probiotic Strains of Lactobacillus paracaseiDiego J Mercanti, Geneviève M Rousseau, María L Capra, et al.
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