Localization of Jacobsen syndrome breakpoints on a 40-Mb physical map of distal chromosome 11q (Q31917682)

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9 December 2019

title

Localization of Jacobsen syndrome breakpoints on a 40-Mb physical map of distal chromosome 11q (English)

1 reference

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9 December 2019

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A Tunnacliffe

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9 December 2019

C Jones

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9 December 2019

D Le Paslier

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9 December 2019

R Todd

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9 December 2019

D Cherif

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9 December 2019

M Birdsall

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9 December 2019

L Devenish

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9 December 2019

C Yousry

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9 December 2019

F E Cotter

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9 December 2019

M R James

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9 December 2019

language of work or name

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1 January 1999

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9 December 2019

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9 December 2019

volume

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9 December 2019

issue

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9 December 2019

page(s)

44-52

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11q23.1 and 11q25-qter YACs suppress tumour growth in vivo.

9 December 2019

cites work

1 reference

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Dynamic mutation: possible mechanisms and significance in human disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

A High-Resolution STS, EST, and Gene-Based Physical Map of the Hereditary Paraganglioma Region on Chromosome 11q23

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

Molecular cytogenetic delineation of a novel critical genomic region in chromosome bands 11q22.3-923.1 in lymphoproliferative disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

A first-generation physical map of the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

A radiation hybrid map of 506 STS markers spanning human chromosome 11.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

Clinical and molecular characterization of patients with distal 11q deletions.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet alpha-granules and chromosome 11 deletion at 11q23.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

21 June 2018

1 reference

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A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones

21 June 2018

1 reference

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Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310705

Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3.

31 October 2018

1 reference

12 December 2020

Hunting 11q23 deletions with fluorescence in situ hybridization (FISH)

1 reference

12 December 2020

A yeast artificial chromosome contig and NotI restriction map that spans the tumor suppressor gene(s) locus, 11q22.2-q23.3.

1 reference

12 December 2020

Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes

1 reference

12 December 2020

11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis

1 reference

12 December 2020

Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B

1 reference

12 December 2020

Identifiers

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9 December 2019

PubMed publication ID

9927483

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