Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data. | BMC Proc;5 Suppl 9: S96, 2011 Nov 29. | MEDLINE

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Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data.

Kraja, Aldi T; Czajkowski, Jacek; Feitosa, Mary F; Borecki, Ingrid B; Province, Michael A.

Affiliation

Kraja AT; Division of Statistical Genomics, Center for Genome Sciences & Systems Biology, Washington University School of Medicine, 4444 Forest Park Boulevard, St, Louis, MO 63110, USA. aldi@wustl.edu.

BMC Proc ; 5 Suppl 9: S96, 2011 Nov 29.

Article in En | MEDLINE | ID: mdl-22373254

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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: BMC Proc Year: 2011 Document type: Article Affiliation country: United States Country of publication: United kingdom

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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: BMC Proc Year: 2011 Document type: Article Affiliation country: United States Country of publication: United kingdom