Association between the ABO locus and hematological traits in Korean. - Wikidata - wikimedia - TriplyDB

Association between the ABO locus and hematological traits in Korean.

Association between the ABO locus and hematological traits in Korean.

http://www.wikidata.org/entity/Q34410189

about

Genome-wide association study for endothelial growth factors Association of ABO and Colton Blood Group Gene Polymorphisms With Hematological Traits Variation.Replication and Characterization of Association between ABO SNPs and Red Blood Cell Traits by Meta-Analysis in Europeans.Influence of ABO genotype and phenotype on angiotensin-converting enzyme plasma activity.

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P2860

Association between the ABO locus and hematological traits in Korean.

http://www.wikidata.org/entity/Q34410189

description

2012 nî lūn-bûn

@nan

2012 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

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2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Association between the ABO locus and hematological traits in Korean.

@ast

Association between the ABO locus and hematological traits in Korean.

@en

Association between the ABO locus and hematological traits in Korean.

@nl

type

label

Association between the ABO locus and hematological traits in Korean.

@ast

Association between the ABO locus and hematological traits in Korean.

@en

Association between the ABO locus and hematological traits in Korean.

@nl

prefLabel

Association between the ABO locus and hematological traits in Korean.

@ast

Association between the ABO locus and hematological traits in Korean.

@en

Association between the ABO locus and hematological traits in Korean.

@nl

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Association between the ABO locus and hematological traits in Korean.

@en

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Bong-Jo Kim

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Cheong-sik Kim

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Dong-Joon Kim

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Kyung-Won Hong

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Sanghoon Moon

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Sung Soo Kim

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Young Jin Kim

http://www.w3.org/2001/XMLSchema#string

Yun Kyoung Kim

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P2860

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

PLINK: a tool set for whole-genome association and population-based linkage analyses

Haploview: analysis and visualization of LD and haplotype maps

Origins and functional impact of copy number variation in the human genome

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

Integrated detection and population-genetic analysis of SNPs and copy number variation

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Genotype, haplotype and copy-number variation in worldwide human populations

The genetical structure of populations

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