(Q24545276)

6 July 2017

title

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays (English)

1 reference

6 July 2017

Jan O Korbel

2

0 references

Mark Bender Gerstein

10

object named as

Mark B Gerstein

1 reference

6 July 2017

12

Michael Snyder

1 reference

6 July 2017

1

Alexander Eckehart Urban

1 reference

6 July 2017

11

Sherman M Weissman

1 reference

6 July 2017

9

Beverly S Emanuel

1 reference

6 July 2017

Rebecca Selzer

3

1 reference

6 July 2017

Todd Richmond

4

1 reference

6 July 2017

April Hacker

5

1 reference

6 July 2017

George V Popescu

6

1 reference

6 July 2017

Joseph F Cubells

7

1 reference

6 July 2017

Roland Green

8

1 reference

6 July 2017

language of work or name

English

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publication date

14 March 2006

1 reference

Proceedings of the National Academy of Sciences of the United States of America

6 July 2017

published in

1 reference

6 July 2017

volume

103

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6 July 2017

issue

12

1 reference

6 July 2017

page(s)

4534-4539

1 reference

Recent segmental and gene duplications in the mouse genome

6 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Gene expression analysis using oligonucleotide arrays produced by maskless photolithography

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

A new non-linear normalization method for reducing variability in DNA microarray experiments

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Genomic disorders on 22q11

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Initial sequence of the chimpanzee genome and comparison with the human genome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Fine-scale structural variation of the human genome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Detection of large-scale variation in the human genome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Segmental duplications and copy-number variation in the human genome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Large-scale copy number polymorphism in the human genome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Chromosomal microdeletions: dissecting del22q11 syndrome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Global identification of human transcribed sequences with genome tiling arrays

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

The new cytogenetics: blurring the boundaries with molecular biology

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

High-resolution global profiling of genomic alterations with long oligonucleotide microarray

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Light-directed 5'-->3' synthesis of complex oligonucleotide microarrays

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Segmental duplications: an 'expanding' role in genomic instability and disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Compact encoding strategies for DNA sequence similarity search

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1450206

Molecular genetic confirmatory testing from newborn screening samples for the common African-American, Asian Indian, Southeast Asian, and Chinese beta-thalassemia mutations

27 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0511340103

Application of ROMA (representational oligonucleotide microarray analysis) to patients with cytogenetic rearrangements

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0511340103

21 January 2018

Identifiers

DOI

10.1073/PNAS.0511340103

1 reference

release_jvcxfphxajhevagbptci3zeipu

6 July 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jvcxfphxajhevagbptci3zeipu

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

1450206

1 reference

6 July 2017

1 reference