Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions.
about
Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype.Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat.Techniques for detecting chromosomal aberrations in myelodysplastic syndromesCorrection: Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions.
P2860
Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions.
description
2014 nî lūn-bûn
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2014年の論文
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2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
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2014年論文
@zh-tw
2014年论文
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2014年论文
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2014年论文
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name
Identifying Human Genome-Wide ...... equencing of Selected Regions.
@ast
Identifying Human Genome-Wide ...... equencing of Selected Regions.
@en
type
label
Identifying Human Genome-Wide ...... equencing of Selected Regions.
@ast
Identifying Human Genome-Wide ...... equencing of Selected Regions.
@en
prefLabel
Identifying Human Genome-Wide ...... equencing of Selected Regions.
@ast
Identifying Human Genome-Wide ...... equencing of Selected Regions.
@en
P2093
P2860
P1433
P1476
Identifying Human Genome-Wide ...... equencing of Selected Regions.
@en
P2093
Hongzhi Cao
Jinliang Li
Wenying Guo
P2860
P304
P356
10.1371/JOURNAL.PONE.0123081
P407
P577
2014-01-01T00:00:00Z