Eight closely linked loci place the Wilson disease locus within 13q14-q21. (Q35247717)

7 August 2017

title

Eight closely linked loci place the Wilson disease locus within 13q14-q21. (English)

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7 August 2017

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A M Bowcock

1

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7 August 2017

L A Farrer

2

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7 August 2017

J M Hebert

3

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7 August 2017

M Agger

4

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7 August 2017

I Sternlieb

5

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7 August 2017

I H Scheinberg

6

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7 August 2017

C H Buys

7

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7 August 2017

H Scheffer

8

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7 August 2017

M Frydman

9

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7 August 2017

T Chajek-Saul

10

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7 August 2017

language of work or name

English

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publication date

1 November 1988

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

43

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7 August 2017

issue

5

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7 August 2017

page(s)

664-674

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A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes

7 August 2017

cites work

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Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus.

12 July 2018

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Strategies for multilocus linkage analysis in humans

12 July 2018

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Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13

12 July 2018

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

12 July 2018

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A genetic study of Wilson's disease: evidence for heterogeneity

12 July 2018

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Esterase D: a new human polymorphism

12 July 2018

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Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

12 July 2018

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Mapping of seven polymorphic loci on human chromosome 13 by in situ hybridization

12 July 2018

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Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715529

Human retinoblastoma susceptibility gene: cloning, identification, and sequence

12 July 2018

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A four-allele RFLP identified by an anonymous single copy genomic clone at 13q21-13qter [HGM8 assignment no. D13S12]

12 July 2018

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A genetic linkage map of the human genome.

12 July 2018

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A primary genetic linkage map for human chromosome 12.

12 July 2018

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Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.

12 July 2018

1 reference

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A primary genetic map of chromosome 13q.

12 July 2018

1 reference

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Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma

12 July 2018

1 reference

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Evidence for linkage between Wilson disease and esterase D in three kindreds: detection of linkage for an autosomal recessive disorder by the family study method.

12 July 2018

1 reference

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Linkage of the Wilson disease gene to chromosome 13 in North-American pedigrees

12 July 2018

1 reference

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Re-evaluation of the sublocalization of esterase D and its relation to the retinoblastoma locus by in situ hybridization

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715529

Evidence for increased recombination near the human insulin gene: implication for disease association studies

12 July 2018

1 reference

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Construction of linkage maps with DNA markers for human chromosomes.

12 July 2018

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Polymorphisms revealed by random probe H2-10 [D13S26] which maps to chromosome 13q21-q22.

12 July 2018

1 reference

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Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715529

An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715529

A high frequency RFLP identified by an anonymous single copy genomic clone at 13q14.1-13q14.2 [HGM8 assignment no. D13S22].

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715529

A straightforward approach to isolate DNA sequences with potential linkage to the retinoblastoma locus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715529

Retinoblastoma and Subband Deletion of Chromosome 13

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715529

Diagnosis of Treatable Wilson's Disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715529

Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715529

A new human RFLP identified by 7D2 places D13S10 proximal to esterase D

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715529

Prediction of the Risk of Hereditary Retinoblastoma, Using DNA Polymorphisms within the Retinoblastoma Gene

26 September 2018

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12 December 2020

Prevention of Wilson's Disease in Asymptomatic Patients

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12 December 2020

Progress in mapping human autosomes

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12 December 2020

Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14

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12 December 2020

Report of the Committee on Methods of Linkage Analysis and Reporting

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12 December 2020

Close linkage of MT2P1 with GC on chromosome 4

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12 December 2020

Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma

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12 December 2020

Development of a map of chromosome 11p

1 reference

12 December 2020

Identifiers

PMC publication ID

1715529

1 reference

7 August 2017

1 reference