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Serveur d'exploration sur les relations entre la France et l'Australie - Analysis (UK)

Index « Auteurs » - entrée « Robert D. S. Pitceathly »
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Robert D. Reed < Robert D. S. Pitceathly < Robert D. Schnabel  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 1.
Ident.Authors (with country if any)Title
001D92 (2012) Joanna L. Elson [Royaume-Uni] ; Mary G. Sweeney [Royaume-Uni] ; Vincent Procaccio [France] ; John W. Yarham [Royaume-Uni] ; Antonio Salas [Espagne] ; Qing-Peng Kong [République populaire de Chine] ; Francois H. Van Der Westhuizen [Afrique du Sud] ; Robert D. S. Pitceathly [Royaume-Uni] ; David R. Thorburn [Australie] ; Marie T. Lott [États-Unis] ; Douglas C. Wallace [États-Unis] ; Robert W. Taylor [Royaume-Uni] ; Robert Mcfarland [Royaume-Uni]Toward a mtDNA locus‐specific mutation database using the LOVD platform

List of associated KwdEn.i

Nombre de
documents		Descripteur
1Association study
1Bandelt
1Biochem biophys
1Biochemical defect
1Cambridge reference sequence
1Central parkway
1Chinnery
1Clinical diagnosis
1Clinical manifestations
1Common disease
1Complete sequences
1Complex disease
1Current databases
1Database
1Disease progression
1Elson
1European mtdnas
1External ophthalmoplegia
1Gene variant databases
1Genet
1Genet elson
1Genet epub
1Genet mcfarland
1Genetic medicine
1Genome
1Genotype
1Haplogroup
1Hgvs guidelines
1Howell
1Human disease
1Human health
1Human mitochondrial
1Human mitochondrial genome database
1Human mtdna
1Human mutation
1Human variome project
1Hypertrophic cardiomyopathy
1Initiation codon
1Lovd
1Lovd database
1Lovd platform
1Many sequences
1Many years
1Mcfarland
1Medical research council
1Mitochondrial
1Mitochondrial disease
1Mitochondrial disorders
1Mitochondrial genome
1Mitochondrial research group
1Mitochondrial trna mutations
1Mitomap
1Modular design
1Mtdna
1Mtdna changes
1Mtdna disease
1Mtdna haplogroup
1Mtdna mutations
1Mtdna polymorphisms
1Mtdna region
1Mtdna variants
1Mtdna variation
1Multiple copies
1Mutat
1Mutation
1National hospital
1Newcastle university
1Next generation
1Next generation sequencing
1Nucleic acids
1Optic neuropathy
1Pathogenic
1Pathogenic mtdna mutations
1Pathogenic mutation
1Pathogenic mutations
1Pathogenic variant
1Pathogenicity
1Phenotype
1Phylogeographic analysis
1Polymorphism
1Population variants
1Primary mutation
1Research council
1Salas
1Search options
1Sequencing
1Single database
1Single group
1Such data
1Threshold level
1Trna
1Turnbull
1Variant
1Variant pathogenicity
1Wiley periodicals

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