(Q43105372)

14 November 2017

An intronic region within the human factor VIII gene is duplicated within Xq28 and is homologous to the polymorphic locus DXS115 (767). (English)

1 reference

14 November 2017

Patterson M

1

1 reference

14 November 2017

Gitschier J

2

1 reference

14 November 2017

Bloomfield J

3

1 reference

14 November 2017

Bell M

4

1 reference

14 November 2017

Dorkins H

5

1 reference

14 November 2017

Froster-Iskenius U

6

1 reference

14 November 2017

Sommer S

7

1 reference

14 November 2017

Sobell J

8

1 reference

14 November 2017

Schaid D

9

1 reference

14 November 2017

Thibodeau S

10

1 reference

14 November 2017

language of work or name

English

0 references

publication date

1 May 1989

1 reference

American Journal of Human Genetics

14 November 2017

1 reference

14 November 2017

44

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14 November 2017

679-685

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14 November 2017

5

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Easy calculations of lod scores and genetic risks on small computers

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Characterization of the human factor VIII gene.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Detection and sequence of mutations in the factor VIII gene of haemophiliacs

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Resolution of DNA molecules greater than 5 megabases by contour-clamped homogeneous electric fields

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Linkage studies in a large fragile X family

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Detection of specific sequences among DNA fragments separated by gel electrophoresis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715651

Report of the committee on the genetic constitution of the X and Y chromosomes

15 August 2018

1 reference

12 December 2020

Physical mapping studies on the human X chromosome in the region Xq27-Xqter

1 reference

12 December 2020

Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome

1 reference

12 December 2020

Improved DNA markers for efficient analysis of fragile X families

1 reference

12 December 2020

Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.

1 reference

12 December 2020

Identifiers

1 reference

14 November 2017

1 reference