(Q35198479)

English

Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity

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scholarly article

1 reference

Europe PubMed Central

7 August 2017

Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity (English)

1 reference

Europe PubMed Central

7 August 2017

retinitis pigmentosa

1 reference

based on heuristic

inferred from title

author name string

Lester DH

1

1 reference

Europe PubMed Central

7 August 2017

Inglehearn CF

2

1 reference

Europe PubMed Central

7 August 2017

Bashir R

3

1 reference

Europe PubMed Central

7 August 2017

Ackford H

4

1 reference

Europe PubMed Central

7 August 2017

Esakowitz L

5

1 reference

Europe PubMed Central

7 August 2017

Jay M

6

1 reference

Europe PubMed Central

7 August 2017

Bird AC

7

1 reference

Europe PubMed Central

7 August 2017

Wright AF

8

1 reference

Europe PubMed Central

7 August 2017

Papiha SS

9

1 reference

Europe PubMed Central

7 August 2017

Bhattacharya SS

10

1 reference

Europe PubMed Central

7 August 2017

language of work or name

0 references

publication date

1 September 1990

1 reference

Europe PubMed Central

7 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

7 August 2017

47

1 reference

Europe PubMed Central

7 August 2017

3

1 reference

Europe PubMed Central

7 August 2017

536-541

1 reference

Europe PubMed Central

7 August 2017

Rod and cone activity in patients with dominantly inherited retinitis pigmentosa: comparisons between psychophysical and electroretinographic measurements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

Isolation and nucleotide sequence of the gene encoding human rhodopsin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

A study of retinitis pigmentosa in the City of Birmingham. II Clinical and genetic heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

Phosphorylation of nucleic acid by an enzyme from T4 bacteriophage-infected Escherichia coli

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

Removal of repeated sequences from hybridisation probes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

Molecular genetics of inherited variation in human color vision

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

Report of the committee on the genetic constitution of chromosome 3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

A point mutation of the rhodopsin 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=1683865

13 July 2018

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

Retinitis pigmentosa.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

13 July 2018

Two types of visual dysfunction in autosomal dominant retinitis pigmentosa.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683865

26 September 2018

Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3

1 reference

https://pubmed.ncbi.nlm.nih.gov/2393026

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two forms of autosomal dominant primary retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/2393026

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Visual pigment levels in retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/2393026

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominantly inherited retinitis pigmentosa. Visual acuity loss by subtype

1 reference

https://pubmed.ncbi.nlm.nih.gov/2393026

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2393026

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3

1 reference

https://pubmed.ncbi.nlm.nih.gov/2393026

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2393026

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

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