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Nature Genetics|October 1, 1995
Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophyA Helbling-Leclerc, X Zhang, H Topaloglu, et al.Human Molecular Genetics|April 2, 2003
Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndromeFlorence Jobard, Bakar Bouadjar, Frédéric Caux, et al.Genomics|July 15, 1994
Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneityM Medhioub, D Cherif, F Benessy, et al.Neurology|June 1, 1996
Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12A Nechiporuk, I Lopes-Cendes, T Nechiporuk, et al.Human Molecular Genetics|August 1, 1995
Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3M Cruts, H Backhovens, J Theuns, et al.Journal of Bacteriology|March 3, 2009
A conserved gene cluster rules anaerobic oxidative degradation of L-ornithineNuria Fonknechten, Alain Perret, Nadia Perchat, et al.Genome Biology|April 19, 2005
Pilot Anopheles gambiae full-length cDNA study: sequencing and initial characterization of 35,575 clonesShawn M Gomez, Karin Eiglmeier, Beatrice Segurens, et al.Proceedings of the National Academy of Sciences of the United States of America|June 21, 1994
Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer familiesM Nyström-Lahti, P Sistonen, J P Mecklin, et al.Genomics|August 1, 1994
Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome geneV Biancalana, E Trivier, C Weber, et al.Medecine Sciences : M/S|July 7, 2025
[Pierre Tiollais (1934-2024), a pioneer in genetic engineering with a lifelong commitment to the hepatitis B virus]Christian Bréchot, Patrick Charnay, Hugues de Thé, et al.Pageof 46