(Q24675745)

2

0 references

E Tarttelin

3

0 references

M Jay

4

0 references

K Evans

5

0 references

T Moore

6

0 references

S Bhattacharya

7

0 references

C F Inglehearn

American Journal of Human Genetics

8

0 references

language of work or name

English

0 references

publication date

October 1996

0 references

published in

0 references

volume

59

0 references

page(s)

864-71

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issue

4

0 references

cites work

A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Strategies for multilocus linkage analysis in humans

7 April 2017

1 reference

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Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

The 1993-94 Généthon human genetic linkage map

7 April 2017

2 references

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Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Easy calculations of lod scores and genetic risks on small computers

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

When more is less: pathogenesis of glutamine repeat neurodegenerative diseases

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Population genetic studies of retinitis pigmentosa.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Nomenclature for inherited diseases of the retina

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

The UK Human Genome Mapping Project online computing service

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Figures and fantasies: the frequencies of the different genetic forms of retinitis pigmentosa

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914817

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8808602

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A computer program to make linkage analysis with LIPED and LINKAGE easier to perform and less prone to input errors

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8808602