(Q33677984)

28 July 2017

Improved genetic mapping of X linked retinoschisis (English)

1 reference

28 July 2017

N D George

1

1 reference

28 July 2017

S J Payne

2

1 reference

28 July 2017

R M Bill

3

1 reference

28 July 2017

D E Barton

4

1 reference

28 July 2017

A T Moore

5

1 reference

28 July 2017

J R Yates

6

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 November 1996

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

33

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28 July 2017

919-922

1 reference

28 July 2017

11

1 reference

Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease gene

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

A high resolution deletion map of human chromosome Xp22.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

A CA-repeat polymorphism near DXS418 (P122).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

Refinement of the chromosomal position of the X linked juvenile retinoschisis gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

21 June 2018

X linked retinoschisis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

The 1993-94 Généthon human genetic linkage map

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

X-linked congenital retinoschisis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

Refined localization of the gene causing X-linked juvenile retinoschisis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

Contribution to carrier detection and genetic counselling in X linked retinoschisis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050785

A second-generation linkage 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=1050785

X-chromosomal recessive retinoschisis in the Region of Pori. An ophthalmo-genetical analysis of 103 cases

21 June 2018

1 reference

12 December 2020

Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region

1 reference

12 December 2020

Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci

1 reference

12 December 2020

New markers for linkage analysis of X-linked hypophosphataemic rickets

1 reference

12 December 2020

Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1?22.2)

1 reference

12 December 2020

Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene

1 reference

12 December 2020

Sixth International Workshop on Human X Chromosome Mapping 1995. Banff, Alberta, Canada, June 16-18, 1995. Report and abstracts

1 reference

12 December 2020

Congenital retinoschisis

1 reference

12 December 2020

Pathology of Hereditary Juvenile Retinoschisis

1 reference

12 December 2020

Visual acuity in 183 cases of X-chromosomal retinoschisis

1 reference

12 December 2020

Hereditary retinoschisis linkage studies in a family and considerations in genetic counselling

1 reference

12 December 2020

Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome

1 reference

12 December 2020

Psychophysical and electroretinographic findings in X-linked juvenile retinoschisis

1 reference

12 December 2020

DNA linkage analysis of X-linked retinoschisis

1 reference

12 December 2020

Detection of the carrier state of X-linked retinoschisis

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.33.11.919

1 reference

28 July 2017

1 reference

28 July 2017

1 reference