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Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers (Q69837442)

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scientific article published on 01 January 1985

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English	Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers	scientific article published on 01 January 1985

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3858218%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3858218%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

retinitis pigmentosa

1 reference

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author name string

R L Nussbaum

1

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6 October 2019

R A Lewis

2

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Europe PubMed Central

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6 October 2019

J G Lesko

3

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Europe PubMed Central

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6 October 2019

R Ferrell

4

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6 October 2019

publication date

1 January 1985

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6 October 2019

language of work or name

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1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3858218%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

70

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Europe PubMed Central

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6 October 2019

1

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Europe PubMed Central

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6 October 2019

45-50

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Europe PubMed Central

PubMed publication ID

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6 October 2019

An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

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A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage studies in X-linked retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electroretinographic testing as an aid in detection of carriers of X-chromosome-linked retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SEX-LINKED OCULAR DISORDERS: TRAIT EXPRESSIVITY IN MALES AND CARRIER FEMALES

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping X-linked ophthalmic diseases. Provisional assignment of the locus for choroideremia to Xq13-q24

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of retinitis pigmentosa in Maine

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and DNA sequence of a full-length cDNA clone for human X chromosome-encoded phosphoglycerate kinase

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of the cDNA coding for rat ornithine transcarbamoylase

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked retinitis pigmentosa and linkage studies with the Xg blood-groups

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rod and cone responses in sex-linked retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human ornithine transcarbamylase locus mapped to band Xp21.1 near the Duchenne muscular dystrophy locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human hypoxanthine-guanine phosphoribosyltransferase. Demonstration of structural variants in lymphoblastoid cells derived from patients with a deficiency of the enzyme

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Choroido-retinal dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3858218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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