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Tags: 2001, American Journal Of Human Genetics, Backlog, Base Sequence, Chromosome Mapping, Chromosomes, Cytochrome-c Oxidase Deficiency, Daly MJ, Delmonte T, Disease Specific, DNA Mutational Analysis, DNA/chemistry/genetics, Electron Transport Complex IV/genetics, Family Health, Female, Gene Frequency, Genes/genetics, Genome, Haplotypes, Hudson TJ, Human, Humans, Journal Article, Lander ES, Lee N, Leigh Disease/enzymology/genetics, Linkage Disequilibrium, Male, Microsatellite Repeats, Mitchell GA, Molecular Sequence Data, Morin CC, Mutation, Pair 2/genetics, Pedigree, Polymorphism, Rioux JD, Robinson BH, Single Nucleotide, Xu F
Tags: 2007, Andria G, Backlog, Boltshauser E, Bowsher D, Chromosome Mapping, Chromosomes, Clinical Genetics, Codon, Congenital/genetics, Cox J, Dimon JH, DNA Mutational Analysis, Donaldson G, Dube MP, Duff A, Female, Founder Effect, Frameshift Mutation, Fraser R, Genetics, Goldberg YP, Green R, Grinspan GA, Haplotypes, Hayden MR, Hossain S, Human, Humans, Ives E, Journal Article, Kerdraon J, MacDonald ML, MacFarlane J, Male, Mattice M, Mutation, Nonsense, Pain Insensitivity, Pair 2/genetics, Pape T, Payne B, Pedigree, Pimstone SN, Population, Radomski C, Samuels ME, Sequence Deletion, Sherrington R, Sibley BG, Sodium Channels/genetics, Thompson J, Toscano E, Young C, Younghusband HB
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