Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes.

Glatt, C E; DeYoung, J A; Delgado, S; Service, S K; Giacomini, K M; Edwards, R H; Risch, N; Freimer, N B

Glatt, C E; DeYoung, J A; Delgado, S; Service, S K; Giacomini, K M; Edwards, R H; Risch, N; Freimer, N B.

Affiliation

Glatt CE; Neurogenetics Laboratory, Program in Human Genetics, University of California San Francisco, San Francisco, California, USA.

Nat Genet ; 27(4): 435-8, 2001 Apr.

Article in En | MEDLINE | ID: mdl-11279528

Subject(s)

Gene Frequency; Genetic Testing; Alleles; DNA Primers; Humans; Molecular Sequence Data; Polymerase Chain Reaction; Polymorphism, Single Nucleotide

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Database: MEDLINE Main subject: Genetic Testing / Gene Frequency Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Humans Language: En Year: 2001 Type: Article

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