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Identifiant IdRef : 154374717Copier cet identifiant (PPN)
Notice de type FMeSH

Point d'accès autorisé

Études d'associations génétiques

Variantes de point d'accès

Association Studies, Genetic
[Nom commun]
Association Study, Genetic
[Nom commun]
Genetic Association Study
[Nom commun]
Studies, Genetic Association
[Nom commun]
Study, Genetic Association
[Nom commun]
Études d'association génétique
[Nom commun]
Genotype-Phenotype Associations
[Nom commun]
Association, Genotype-Phenotype
[Nom commun]
Associations, Genotype-Phenotype
[Nom commun]
Genotype Phenotype Associations
[Nom commun]
Genotype-Phenotype Correlation
[Nom commun]
Genotype Phenotype Correlation
[Nom commun]
Genotype-Phenotype Correlations
[Nom commun]
Correlation, Genotype-Phenotype
[Nom commun]
Correlations, Genotype-Phenotype
[Nom commun]
Genotype Phenotype Correlations
[Nom commun]
Genotype-Phenotype Association
[Nom commun]
Genotype Phenotype Association
[Nom commun]
Candidate Gene Analysis
[Nom commun]
Analyses, Candidate Gene
[Nom commun]
Analysis, Candidate Gene
[Nom commun]
Candidate Gene Analyses
[Nom commun]
Gene Analyses, Candidate
[Nom commun]
Gene Analysis, Candidate
[Nom commun]
Candidate Gene Identification
[Nom commun]
Gene Identification, Candidate
[Nom commun]
Identification, Candidate Gene
[Nom commun]
Candidate Gene Association Study
[Nom commun]
Gene Discovery
[Nom commun]
Discovery, Gene
[Nom commun]
Candidate Gene Association Studies
[Nom commun]
Associations génotype-phénotype
[Nom commun]
Corrélations génotype-phénotype
[Nom commun]
Analyse de gène candidat
[Nom commun]
Identification de gène candidat
[Nom commun]
Découverte de gène
[Nom commun]
Étude d'association de gène candidat
[Nom commun]
Études d'association génétique
[Nom commun]

Informations

Note publique d''information : 
The analysis of a sequence such as a region of a chromosome, a haplotype, a gene, or an allele for its involvement in controlling the phenotype of a specific trait, metabolic pathway, or disease

Note publique d''information : 
Genetic variants (specific mutations or allelles of genes) and their corresponding phenotypic variations in the trait or the disease which the genes controls

Note publique d''information : 
The verification of association of a candidate gene with a specific trait, metabolic pathway, or disease; and which mutations of a candidate gene are associated with the disease

Note publique d''information : 
The determination of genes suspected to be associated with specific traits, metabolic pathways, or diseases

Point d'accès autorisé parallèle

Genetic Association Studies

Autres identifiants

Identifiant MeSH : mesD056726

Utilisation dans FMeSH

Qualificatifs autorisés : CL / EC / HI / IS / MT / ST / TD / VE / SN / ES2010

Equivalent dans un autre référentiel

... Références liées : ...