Advanced Search (Items only)
Tags: 2008, Abdel-Ghaffar TY, Backlog, Bolz HJ, Child, Congenital/diagnosis/genetics, Ebermann I, Elsayed SM, Elsobky E, Female, Homozygote, Humans, Infant, Journal Article, Liver Diseases/genetics/physiopathology, Male, Mutation, Neurology, Nurnberg G, Nurnberg P, Pain Insensitivity, Pedigree, Sodium Channels/genetics, Syndrome
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
atom, dcmes-xml, json, omeka-xml, rss2