A high-resolution survey of deletion polymorphism in the human genome (Q94465012)

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English	A high-resolution survey of deletion polymorphism in the human genome	No description defined

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scholarly article

1 reference

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Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

title

A high-resolution survey of deletion polymorphism in the human genome (English)

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stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

author

Dan Andrews

series ordinal

2

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stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

Jonathan K. Pritchard

series ordinal

5

object named as

Jonathan K Pritchard

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

author name string

Donald F Conrad

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

Nigel P Carter

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

Matthew E Hurles

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

publication date

4 December 2005

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

published in

Nature Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

volume

38

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

page(s)

75-81

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Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

cites work

Large-scale copy number polymorphism in the human genome

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Detection of large-scale variation in the human genome

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Fine-scale structural variation of the human genome

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Segmental duplications and copy-number variation in the human genome

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7 January 2021

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Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

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The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

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Presence of large deletions in kindreds with autism

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When less is more: gene loss as an engine of evolutionary change

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7 January 2021

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Positional Identification of Microdeletions with Genetic Markers

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7 January 2021

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Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements

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Human diallelic insertion/deletion polymorphisms

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7 January 2021

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Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes

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https://api.crossref.org/works/10.1038%2FNG1697

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7 January 2021

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As normal as normal can be?

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7 January 2021

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Recent segmental duplications in the human genome

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Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios

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Comparison of the genomes of human and mouse lays the foundation of genome zoology

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Common deletions and SNPs are in linkage disequilibrium in the human genome

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Common deletion polymorphisms in the human genome.

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7 January 2021

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Complex SNP-related sequence variation in segmental genome duplications

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

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Identifiers

DOI

10.1038/NG1697

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

PubMed publication ID

16327808

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16327808

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 May 2020

 

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