Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome. (Q24540203)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090893%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome (English)

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12 November 2019

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3

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12 November 2019

author name string

L Edelmann

series ordinal

1

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12 November 2019

R K Pandita

series ordinal

2

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12 November 2019

language of work or name

English

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publication date

1 April 1999

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American Journal of Human Genetics

12 November 2019

published in

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12 November 2019

volume

64

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12 November 2019

page(s)

1076-1086

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12 November 2019

issue

4

1 reference

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Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients

12 November 2019

cites work

1 reference

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Expression of multiple gamma-glutamyltransferase genes in man

24 March 2017

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V7, a novel leukocyte surface protein that participates in T cell activation. II. Molecular cloning and characterization of the V7 gene

24 March 2017

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Identification of a human gamma-glutamyl cleaving enzyme related to, but distinct from, gamma-glutamyl transpeptidase

24 March 2017

1 reference

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A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK

24 March 2017

1 reference

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Interstitial deletion of (17)(p11.2p11.2) in nine patients

24 March 2017

1 reference

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A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

24 March 2017

1 reference

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Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11

24 March 2017

1 reference

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Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patients

27 September 2017

1 reference

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Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.

27 September 2017

1 reference

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

27 September 2017

1 reference

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Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients

27 September 2017

1 reference

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Formation of nuclear bodies in cells overexpressing the nuclear pore protein POM121.

27 September 2017

1 reference

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Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.

27 September 2017

1 reference

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A new bacteriophage P1-derived vector for the propagation of large human DNA fragments

27 September 2017

1 reference

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Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome

27 September 2017

1 reference

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Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377832

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

27 September 2017

1 reference

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The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377832

Information transfer between duplicated chromosomal sequences in mammalian cells involves contiguous regions of DNA.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377832

Duplication of the bcr and gamma-glutamyl transpeptidase genes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377832

Dependence of intrachromosomal recombination in mammalian cells on uninterrupted homology

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377832

Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377832

Deletions and microdeletions of 22q11.2 in velo-cardio-facial 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=1377832

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377832

The organization of the gamma-glutamyl transferase genes and other low copy repeats in human chromosome 22q11.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377832

Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.

30 May 2018

1 reference

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High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions.

30 May 2018

1 reference

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Sex-dependent rearrangements resulting in CMT1A and HNPP.

29 November 2018

1 reference

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A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377832

A high-density YAC contig map of human chromosome 22

29 November 2018

1 reference

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Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints

29 November 2018

1 reference

12 December 2020

Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit

1 reference

12 December 2020

Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17

1 reference

12 December 2020

The organization of the human immunoglobulin lambda gene locus

1 reference

12 December 2020

Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome

1 reference

12 December 2020

A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia

1 reference

12 December 2020

Fused transcript of abl and bcr genes in chronic myelogenous leukaemia

1 reference

12 December 2020

DiGeorge syndrome and 22q11 rearrangements

1 reference

12 December 2020

Linear order of the four BCR-related loci in 22q11

1 reference

12 December 2020

Chromosomal region of the cystic fibrosis gene in yeast artificial chromosomes: a model for human genome mapping

1 reference

12 December 2020

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

12 December 2020

A new concept of the cellular basis of immunity

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F302343

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/302343

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090893%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090893%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference