Whole genome distribution and ethnic differentiation of copy number variation in Caucasian and Asian populations.
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A preliminary study of copy number variation in TibetansThe Growing Importance of CNVs: New Insights for Detection and Clinical InterpretationThe genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population.Copy number variation in the porcine genome inferred from a 60 k SNP BeadChipA map of copy number variations in Chinese populations.UCP2 -866G/A, Ala55Val and UCP3 -55C/T polymorphisms in association with obesity susceptibility - a meta-analysis studyIdentification of both copy number variation-type and constant-type core elements in a large segmental duplication region of the mouse genome.Copy number variation accuracy in genome-wide association studies.Family-Based Benchmarking of Copy Number Variation Detection Software.Genetics of cerebral cavernous malformations: current status and future prospectsA Single-Array-Based Method for Detecting Copy Number Variants Using Affymetrix High Density SNP Arrays and its Application to Breast CancerCNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan SubpopulationsCNV analysis in the Lithuanian population.Association of Higher Defensin β-4 Genomic Copy Numbers with Behçet's Disease in Iraqi Patients.Copy number variation in patients with cervical artery dissection.Association between copy number variations of HLA-DQA1 and ankylosing spondylitis in the Chinese Han population.Ionising radiation and genetic risks. XVI. A genome-based framework for risk estimation in the light of recent advances in genome research.Genetic Imbalance in Patients with Cervical Artery DissectionA genome-wide scan for copy number variations using high-density single nucleotide polymorphism array in Simmental cattle.Overall survival in EGFR mutated non-small-cell lung cancer patients treated with afatinib after EGFR TKI and resistant mechanisms upon disease progression.Array comparative genomic hybridization detects chromosomal abnormalities in hematological cancers that are not detected by conventional cytogenetics.SgD-CNV, a database for common and rare copy number variants in three Asian populations.Classification of pathogenic or benign status of CNVs detected by microarray analysis.Familial cerebral cavernous angiomas: clinical and genetic features in a Chinese family with a frame-shift mutation in the CCM1 gene (krit1).Association study of myelin transcription factor 1-like polymorphisms with schizophrenia in Han Chinese population.
P2860
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P2860
Whole genome distribution and ethnic differentiation of copy number variation in Caucasian and Asian populations.
description
2009 nî lūn-bûn
@nan
2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Whole genome distribution and ...... ucasian and Asian populations.
@ast
Whole genome distribution and ...... ucasian and Asian populations.
@en
type
label
Whole genome distribution and ...... ucasian and Asian populations.
@ast
Whole genome distribution and ...... ucasian and Asian populations.
@en
prefLabel
Whole genome distribution and ...... ucasian and Asian populations.
@ast
Whole genome distribution and ...... ucasian and Asian populations.
@en
P2093
P2860
P50
P1433
P1476
Whole genome distribution and ...... ucasian and Asian populations.
@en
P2093
Betty M Drees
Christopher J Papasian
Hongyi Deng
James J Hamilton
Jing Cheng
Liang Wang
P2860
P356
10.1371/JOURNAL.PONE.0007958
P407
P577
2009-11-23T00:00:00Z