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Brain Research. Gene Expression Patterns|March 17, 2004
Microarray analysis of brain RNA in mice with methylenetetrahydrofolate reductase deficiency and hyperhomocysteinemiaZhoutao Chen, Bing Ge, Thomas J Hudson, et al.Current Protocols in Bioinformatics|April 23, 2008
The Human Gene Mutation Database (HGMD) and its exploitation in the study of mutational mechanismsDavid N Cooper, Peter D Stenson, Nadia A ChuzhanovaPublic Health Genomics|November 30, 2016
The Rise and Rise of Exome SequencingChee-Seng Ku, David N Cooper, George P PatrinosHuman Genetics|February 19, 2017
Emerging genotype-phenotype relationships in patients with large NF1 deletionsHildegard Kehrer-Sawatzki, Victor-Felix Mautner, David N CooperJournal of Medical Genetics|February 12, 2013
From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic diseaseChee-Seng Ku, Eng King Tan, David N CooperHuman Genomics|September 5, 2015
Trans-species polymorphism in humans and the great apes is generally maintained by balancing selection that modulates the host immune responseLuisa Azevedo, Catarina Serrano, Antonio Amorim, et al.World Journal of Gastroenterology|April 20, 2013
Clinical relevance of cancer genome sequencingChee Seng Ku, David N Cooper, Dimitrios H RoukosHuman Genetics|November 10, 2007
Replication of an association between 17q21 SNPs and asthma in a French-Canadian familial collectionAnne-Marie Madore, Karine Tremblay, Thomas J Hudson, et al.The Laryngoscope|March 23, 2023
Airway Resistance and Respiratory Distress in Laryngeal Cancer: A Computational Fluid Dynamics StudyThomas J Hudson, Rayane Ait Oubahou, Luc Mongeau, et al.American Journal of Medical Genetics. Part A|November 4, 2004
Functional analysis of polymorphic variation within the promoter and 5' untranslated region of the neurofibromatosis type 1 (NF1) geneMartin P Horan, Michael Osborn, David N Cooper, et al.Pageof 57