Recombination of 4p16 DNA markers in an unusual family with Huntington disease. (Q35195406)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1350884%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

title

Recombination of 4p16 DNA markers in an unusual family with Huntington disease (English)

1 reference

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18 September 2019

0 references

1

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Margaret A. Pericak-Vance

18 September 2019

5

object named as

Pericak-Vance MA

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18 September 2019

7

Roses AD

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18 September 2019

author name string

Zhu N

2

1 reference

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18 September 2019

Zuo J

3

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18 September 2019

Bull L

4

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18 September 2019

Vance JM

6

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18 September 2019

Milatovich A

8

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18 September 2019

Francke U

9

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18 September 2019

Cox DR

10

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18 September 2019

publication date

1 June 1992

1 reference

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American Journal of Human Genetics

18 September 2019

language of work or name

English

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published in

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18 September 2019

volume

50

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18 September 2019

issue

6

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18 September 2019

page(s)

1218-1230

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Strategies for multilocus linkage analysis in humans

18 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

A polymorphic DNA marker genetically linked to Huntington's disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

The mutation rate to Huntington's chorea

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Recombinant fragment assay for gene targetting based on the polymerase chain reaction

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

A highly polymorphic locus very tightly linked to the Huntington's disease gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

A DNA probe, D5 [D4S90] mapping to human chromosome 4p16.3.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Recombination events suggest potential sites for the Huntington's disease gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Characterization of eight VNTR loci by agarose gel electrophoresis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Huntington disease: no evidence for locus heterogeneity

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene

13 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

13 July 2018

https://pubmed.ncbi.nlm.nih.gov/1350884

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Linkage disequilibrium in Huntington's disease: an improved localisation for the gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Isolation and field-inversion gel electrophoresis analysis of DNA markers located close to the Huntington disease gene.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Segregation of the Huntington disease region of human chromosome 4 in a somatic cell hybrid

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Dinucleotide repeat polymorphism located at D21S120.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

A cloned DNA segment from the telomeric region of human chromosome 4p is not detectably rearranged in Huntington disease patients

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Dinucleotide repeat polymorphism located at D4S169.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Linkage disequilibrium and recombination make a telomeric site for the Huntington's disease gene unlikely

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Defined physical limits of the Huntington disease gene candidate region

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Complex patterns of linkage disequilibrium in the Huntington disease region

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Characterization and rapid analysis of the highly polymorphic VNTR locus D4S125 (YNZ32), closely linked to the Huntington disease gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Linkage disequilibrium and modification of risk for Huntington disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

Mapping of cosmid clones in Huntington's disease region of chromosome 4.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682573

A sequence in M13 phage detects hypervariable minisatellites in human and animal DNA

13 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1350884

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Analysis of somatic mutations at human minisatellite loci in tumors and cell lines

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1350884

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1350884%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

PubMed publication ID

1350884

1 reference