(Q80962747)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15526218%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

title

Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15526218%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

2

James R Lupski

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15526218%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

author name string

Christine J Shaw

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15526218%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

publication date

22 October 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15526218%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

number of pages

7

1 reference

inferred from page(s)

published in

Human Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15526218%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

volume

116

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15526218%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

page(s)

1-7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15526218%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

issue

1-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15526218%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00439-004-1204-9

4 January 2020

exact match

0 references

cites work

Generation of a widespread Drosophila inversion by a transposable element.

1 reference

12 December 2020

Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2.

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Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions

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Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

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Analysis of 22 deletion breakpoints in dystrophin intron 49.

1 reference

12 December 2020

The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

1 reference

12 December 2020

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

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12 December 2020

Genome rearrangements by nonlinear transposons in maize

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12 December 2020

Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females

1 reference

12 December 2020

Hotspots of homologous recombination in the human genome: not all homologous sequences are equal

1 reference

12 December 2020

Mechanism and regulation of human non-homologous DNA end-joining

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12 December 2020

Genome architecture, rearrangements and genomic disorders

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12 December 2020

Alu repeats and human disease

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12 December 2020

Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution

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12 December 2020

Gross chromosome rearrangements mediated by transposable elements in Drosophila melanogaster

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12 December 2020

Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2.

1 reference

12 December 2020

Uncommon deletions of the Smith-Magenis syndrome region can be recurrent when alternate low-copy repeats act as homologous recombination substrates

1 reference

12 December 2020

Serial segmental duplications during primate evolution result in complex human genome architecture

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12 December 2020

An Alu Transposition Model for the Origin and Expansion of Human Segmental Duplications

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12 December 2020

Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene.

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Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

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12 December 2020

Genome architecture catalyzes nonrecurrent chromosomal rearrangements

1 reference

12 December 2020

Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p

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12 December 2020

Mobile elements: drivers of genome evolution

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12 December 2020

Initial sequencing and analysis of the human genome

1 reference

12 December 2020