(Q53585955)

15 May 2018

title

New insights into the biological basis of genomic disorders. (English)

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15 May 2018

author

Simon Myers

series ordinal

1

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15 May 2018

Steven A McCarroll

series ordinal

2

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15 May 2018

language of work or name

English

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publication date

1 December 2006

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15 May 2018

published in

Nature Genetics

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15 May 2018

volume

38

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15 May 2018

page(s)

1363-1364

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15 May 2018

issue

12

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15 May 2018

https://scigraph.springernature.com/pub.10.1038/ng1206-1363

exact match

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cites work

Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

The fine-scale structure of recombination rate variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

Intense and highly localized gene conversion activity in human meiotic crossover hot spots

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

Comparison of fine-scale recombination rates in humans and chimpanzees.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

Fine-scale recombination patterns differ between chimpanzees and humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

Common deletion polymorphisms in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

A fine-scale map of recombination rates and hotspots across the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1206-1363

21 January 2018

Identifiers

DOI

10.1038/NG1206-1363

1 reference

15 May 2018

PubMed ID

17133221

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15 May 2018