Shared genomic segment analysis: the power to find rare disease variants
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Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees.FamPipe: An Automatic Analysis Pipeline for Analyzing Sequencing Data in Families for Disease StudiesAnalysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31.Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.Reparameterization of PAM50 expression identifies novel breast tumor dimensions and leads to discovery of a genomewide significant breast cancer locus at 12q15.
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Shared genomic segment analysis: the power to find rare disease variants
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 19 September 2012
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vedecký článok
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vetenskaplig artikel
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Shared genomic segment analysis: the power to find rare disease variants
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Shared genomic segment analysis: the power to find rare disease variants.
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Shared genomic segment analysis: the power to find rare disease variants
@en
Shared genomic segment analysis: the power to find rare disease variants.
@nl
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Shared genomic segment analysis: the power to find rare disease variants
@en
Shared genomic segment analysis: the power to find rare disease variants.
@nl
P2093
P2860
P1476
Shared genomic segment analysis: the power to find rare disease variants
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P2093
Deborah W Neklason
Haley J Abel
Nicola J Camp
Randall W Burt
Ryan P Abo
Therese M Tuohy
P2860
P304
P356
10.1111/J.1469-1809.2012.00728.X
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P577
2012-09-19T00:00:00Z