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

Index « Auteurs » - entrée « Elizabeth Freitas »
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Elizabeth Fontham < Elizabeth Freitas < Elizabeth G. Holliday  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 1.
Ident.Authors (with country if any)Title
003454 (2003) Michael Hunter [Australie] ; Rafaëlle Bernard [France] ; Elizabeth Freitas [Australie] ; Amandine Boyer [France] ; Bharti Morar [Australie] ; Ian J. Martins [Australie] ; Ivailo Tournev [Bulgarie] ; Albena Jordanova [Bulgarie] ; Velina Guergelcheva [Bulgarie] ; Boryana Ishpekova [Bulgarie] ; Ivo Kremensky [Bulgarie] ; Garth Nicholson [Australie] ; Beate Schlotter [Allemagne] ; Hanns Lochmüller [Allemagne] ; Thomas Voit [Allemagne] ; Jaume Colomer [Espagne] ; P. K. Thomas [Royaume-Uni] ; Nicolas Levy [France] ; Luba Kalaydjieva [Australie]Mutation screening of the N‐myc downstream‐regulated gene 1 (NDRG1) in patients with Charcot‐Marie‐Tooth Disease

List of associated KwdEn.i

Nombre de
documents
Descripteur
1Amino acids
1Autosomal
1Autosomal recessive
1Cdna
1Cellular stress
1Clifton hill
1Clinical phenotypes
1Coding
1Coding region
1Coding sequence
1Common causes
1Database
1Demyelinating
1Demyelinating neuropathies
1Different mutations
1Differential display analysis
1Disease table
1Early growth response
1Early onset
1Exon
1Founder mutation
1Gene
1Genetique medicale
1Hearing loss
1Hereditary
1Hereditary motor
1High degree
1Hmsnl
1Homozygous state
1Human genes
1Intronic sequences
1Kalaydjieva
1Lower limbs
1Lupski
1Medical research
1Medical university
1Molecular pathogenesis
1Mutation
1Mutation screening
1Ndrg1
1Ndrg1 coding sequence
1Ndrg1 mutations
1Neuropathy
1Neuropathy type
1Novel demyelinating neuropathy
1Novel gene
1Novel mutation
1Nucleotide
1Nucleotide diversity
1Peripheral nerve
1Peripheral neuropathies
1Peripheral neuropathy
1Perkin biosystems
1Phenotype
1Primer
1Recessive
1Romani
1Same time
1Sensory neuropathy
1Sequence analysis
1Sequence variant
1Sequence variants
1Sequence variation
1Sequencing
1Sequencing analysis
1Single nucleotide polymorphisms
1Snp
1Tumor suppression
1Unique role
1Unrelated individuals
1Variant

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