(Q34307943)

English

Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia (English)

1 reference

Europe PubMed Central

1 August 2017

author name string

F P Cremers

1

1 reference

Europe PubMed Central

1 August 2017

D J van de Pol

2

1 reference

Europe PubMed Central

1 August 2017

B Wieringa

3

1 reference

Europe PubMed Central

1 August 2017

F S Collins

4

1 reference

Europe PubMed Central

1 August 2017

E M Sankila

5

1 reference

Europe PubMed Central

1 August 2017

V M Siu

6

1 reference

Europe PubMed Central

1 August 2017

W F Flintoff

7

1 reference

Europe PubMed Central

1 August 2017

F Brunsmann

8

1 reference

Europe PubMed Central

1 August 2017

L A Blonden

9

1 reference

Europe PubMed Central

1 August 2017

H H Ropers

10

1 reference

Europe PubMed Central

1 August 2017

language of work or name

0 references

publication date

1 October 1989

1 reference

Europe PubMed Central

1 August 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

1 August 2017

86

1 reference

Europe PubMed Central

1 August 2017

19

1 reference

Europe PubMed Central

1 August 2017

7510-7514

1 reference

Europe PubMed Central

1 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Genomic sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Double cos site vectors: simplified cosmid cloning.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 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=298094

6 July 2018

Directional cloning of DNA fragments at a large distance from an initial probe: a circularization method

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

The sex-determining region of the human Y chromosome encodes a finger protein.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Two different genes for X-linked retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Localisation of the endpoints of deletions in the 5' region of the Duchenne gene using a sequence isolated by chromosome jumping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Construction and use of human chromosome jumping libraries from NotI-digested DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

A highly polymorphic locus in human DNA revealed by cosmid-derived probes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Construction of a NotI linking library and isolation of new markers close to the Huntington's disease gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Preserving primary cDNA libraries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Construction of a general human chromosome jumping library, with application to cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Chromosome jumping from D4S10 (G8) toward the Huntington disease gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=298094

6 July 2018

Choroideremia: further evidence for assignment of the locus to Xq13-Xq21

1 reference

https://pubmed.ncbi.nlm.nih.gov/2798422

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical-genealogical evidence

1 reference

https://pubmed.ncbi.nlm.nih.gov/2798422

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7

1 reference

https://pubmed.ncbi.nlm.nih.gov/2798422

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2798422

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strategies for mapping and cloning macroregions of mammalian genomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2798422

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of the DXS165 locus in patients with classical choroideremia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2798422

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombination between DXS7, DXS84 and a rare form of X-linked retinitis pigmentosa (McK-30320)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2798422

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.86.19.7510

1 reference

Europe PubMed Central

1 August 2017

1989PNAS...86.7510C

0 references

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

ResearchGate publication ID

0 references

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