(Q34346727)

English

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

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

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

1 reference

Europe PubMed Central

1 August 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Nussbaum RL

1

1 reference

Europe PubMed Central

1 August 2017

Lesko JG

2

1 reference

Europe PubMed Central

1 August 2017

Lewis RA

3

1 reference

Europe PubMed Central

1 August 2017

Ledbetter SA

4

1 reference

Europe PubMed Central

1 August 2017

Ledbetter DH

5

1 reference

Europe PubMed Central

1 August 2017

language of work or name

0 references

publication date

1 September 1987

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

84

1 reference

Europe PubMed Central

1 August 2017

6521-6525

1 reference

Europe PubMed Central

1 August 2017

18

1 reference

Europe PubMed Central

1 August 2017

Choroideremia; clinical and genetic aspects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

6 July 2018

Choroideremia, obesity, and congenital deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

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=299109

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=299109

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

6 July 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

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=299109

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=299109

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=299109

6 July 2018

Contiguous gene syndromes: a component of recognizable syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

6 July 2018

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

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=299109

6 July 2018

Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

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=299109

6 July 2018

High Resolution of Human Chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

6 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=299109

6 July 2018

Room temperature method for increasing the rate of DNA reassociation by many thousandfold: the phenol emulsion reassociation technique

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

6 July 2018

Expression of the fragile (X) chromosome in an interspecific somatic cell hybrid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=299109

27 October 2018

A new method for purifying lambda DNA from phage lysates

1 reference

https://pubmed.ncbi.nlm.nih.gov/3476958

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/3476958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3476958

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/3476958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/3476958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved method for G-banding chromosomes after in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/3476958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.84.18.6521

1 reference

Europe PubMed Central

1 August 2017

1987PNAS...84.6521N

0 references

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

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0 references

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