(Q72391041)

English

Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family

scientific article published on 01 January 1995

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7814030%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7814030%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

retinitis pigmentosa

1 reference

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inferred from title

author name string

R E McGuire

1

1 reference

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26 October 2019

A M Gannon

2

1 reference

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26 October 2019

L S Sullivan

3

1 reference

Europe PubMed Central

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26 October 2019

J A Rodriguez

4

1 reference

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26 October 2019

S P Daiger

5

1 reference

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26 October 2019

publication date

1 January 1995

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26 October 2019

1 reference

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26 October 2019

95

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26 October 2019

1

1 reference

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26 October 2019

71-74

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26 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00225078

0 references

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/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second-generation linkage map of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Faster sequential genetic linkage computations

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 1993-94 Généthon human genetic linkage map

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A leucine to arginine amino acid substitution at codon 46 of rhodopsin is responsible for a severe form of autosomal dominant retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

(CA)n-dinucleotide repeat at the PDEB locus in 4p16.3

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8).

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient computations in multilocus linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7814030

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00225078

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7814030%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7814030%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

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