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

Index « Auteurs » - entrée « Sue Richards »
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Sue Price < Sue Richards < Sue Ring  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 1.
Ident.Authors (with country if any)Title
002675 (2010) Maija R. J. Kohonen-Corish [Australie] ; Jumana Y. Al-Aama [Arabie saoudite] ; Arleen D. Auerbach [États-Unis] ; Myles Axton [États-Unis] ; Carol Isaacson Barash [États-Unis] ; Inge Bernstein [Danemark] ; Christophe Béroud [France] ; John Burn [Royaume-Uni] ; Fiona Cunningham [Royaume-Uni] ; Garry R. Cutting [États-Unis] ; Johan T. Den Dunnen [Pays-Bas] ; Marc S. Greenblatt [États-Unis] ; Jim Kaput [États-Unis] ; Michael Katz [États-Unis] ; Annika Lindblom [Suède] ; Finlay Macrae ; Donna Maglott [États-Unis] ; Gabriela Möslein [Allemagne] ; Sue Povey [Royaume-Uni] ; Raj Ramesar [Afrique du Sud] ; Sue Richards [États-Unis] ; Daniela Seminara [États-Unis] ; María-Jesús Sobrido [Espagne] ; Sean Tavtigian [États-Unis] ; Graham Taylor [Royaume-Uni] ; Mauno Vihinen [Finlande] ; Ingrid Winship [Australie] ; Richard G. H. Cotton [Australie]How to catch all those mutations—the report of the Third Human Variome Project Meeting, UNESCO Paris, May 2010

List of associated KwdEn.i

Nombre de
documents		Descripteur
1Access data
1Advance variation data collection
1American college
1Biotechnology information
1Central databases
1Classification system
1Clinical data
1Clinical geneticists
1Clinical genetics
1Colorectal cancers
1Complex sequence variants
1Consortium
1Copy number variant
1Country node
1Curation
1Curator
1Current framework
1Data collection
1Data transfer
1Data types
1Database
1Database curators
1Dbsnp reference numbers
1Digital identifier
1Disparate groups
1Easy integration
1Ethical issues
1Family data
1First meeting
1Full report
1Funding
1Funding mechanisms
1Garvan institute
1Gen2phen project
1Genet cotton
1Genetic
1Genetic disease
1Genetic knowledge
1Genetic medicine
1Genetic variants
1Genetic variation
1Genetic variations
1Genetics
1Genome
1Genomic disorders research center
1Genotype
1Healthcare
1Hereditary breast
1Hgnc gene names
1Hgvs
1Hgvs nomenclature
1Hgvs recommendations
1Hgvs website
1Human disease
1Human genetics
1Human genome
1Human genome project
1Human health
1Human mutation
1Human variome
1Human variome project
1Human variome project meeting
1Iarc system
1Identifier
1International society
1Knowledge base
1Locus reference genomic
1Lsdb
1Lsdb object model
1Lsdbs
1Medical genetics
1Medical research
1Meeting report
1Melbourne
1Micronutrient genomics project
1Molecular medicine
1Mutation
1Mutation data
1Mutation databases
1National center
1Natural successor
1Neurogenetics consortium
1Node
1Ontology
1Other resources
1Overall data integration
1Pathogenicity
1Phenotype
1Phenotype information
1Phenotypic data
1Pilot study
1Public databases
1Quality control
1Rare disorders
1Robust process
1Royal melbourne hospital
1Sequence format
1Sequence variants
1Software tools
1Unclassified variants

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