(Q35205608)

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Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array

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scholarly article

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Europe PubMed Central

PubMed publication ID

7 August 2017

Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array (English)

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Europe PubMed Central

PubMed publication ID

7 August 2017

esophageal squamous cell carcinoma

1 reference

based on heuristic

inferred from title

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author name string

Nan Hu

1

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Europe PubMed Central

PubMed publication ID

7 August 2017

Chaoyu Wang

2

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Europe PubMed Central

PubMed publication ID

7 August 2017

Ying Hu

3

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Europe PubMed Central

PubMed publication ID

7 August 2017

Howard H Yang

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Li-Hui Kong

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Ning Lu

6

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Hua Su

7

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Quan-Hong Wang

8

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Alisa M Goldstein

9

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Kenneth H Buetow

10

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Michael R Emmert-Buck

11

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Europe PubMed Central

PubMed publication ID

7 August 2017

Philip R Taylor

12

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7 August 2017

Maxwell P Lee

13

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7 August 2017

language of work or name

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publication date

29 November 2006

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Europe PubMed Central

PubMed publication ID

7 August 2017

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Europe PubMed Central

PubMed publication ID

7 August 2017

7

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Europe PubMed Central

PubMed publication ID

7 August 2017

299

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

copyright license

Creative Commons Attribution 2.0 Generic

29 November 2006

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April 2022 Public Data File from Crossref

copyright status

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April 2022 Public Data File from Crossref

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High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines

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1 reference

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13 July 2018

Genetic progression and heterogeneity associated with the development of esophageal squamous cell carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1687196

13 July 2018

High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern China

1 reference

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13 July 2018

Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer

1 reference

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13 July 2018

Laser capture microdissection

1 reference

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13 July 2018

Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis.

1 reference

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26 September 2018

High-resolution analysis of chromosomal imbalances using the Affymetrix 10K SNP genotyping chip.

1 reference

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Epidemiology of esophageal cancer in China.

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26 September 2018

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Allelotyping of esophageal squamous-cell carcinoma on chromosome 13 defines deletions related to family history

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Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/17134496

12 December 2020

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1 reference

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Genome-wide association study in esophageal cancer using GeneChip mapping 10K array

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2164-7-299

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

ResearchGate publication ID

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