New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization. (Q35247023)

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1 October 2019

title

New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization (English)

1 reference

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1 October 2019

author name string

R E Schnur

1

1 reference

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1 October 2019

S A Ledbetter

2

1 reference

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1 October 2019

D H Ledbetter

3

1 reference

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1 October 2019

D E Merry

4

1 reference

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1 October 2019

R L Nussbaum

5

1 reference

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1 October 2019

language of work or name

English

0 references

publication date

1 February 1989

1 reference

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American Journal of Human Genetics

1 October 2019

published in

1 reference

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1 October 2019

volume

44

1 reference

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1 October 2019

issue

2

1 reference

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1 October 2019

page(s)

248-254

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describes a project that uses

1 October 2019

in situ hybridization

1 reference

A cytological map of the human X chromosome--evidence for non-random recombination

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

Implications of fragile X expression in normal males for the nature of the mutation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

Fragile X syndrome: a unique mutation in man.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

Linkage studies in a large fragile X family

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

RFLP for linkage analysis of fragile X syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

Screening λgt Recombinant Clones by Hybridization to Single Plaques in Situ

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

Further evidence for genetic heterogeneity in the fragile X syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715401

Physical mapping studies on the human X chromosome in the region Xq27-Xqter

26 September 2018

1 reference

12 December 2020

Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.

1 reference

12 December 2020

Report of the committee on the genetic constitution of the X and Y chromosomes

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic linkage heterogeneity in the fragile X syndrome

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563194%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

PubMed publication ID

2563194

1 reference