(Q33373107)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

title

Isolation of a human DNA sequence which spans the fragile X (English)

1 reference

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19 September 2019

1

1 reference

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19 September 2019

Valentine Hyland

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

author name string

Yu S

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

Pritchard M

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

Nagaraja R

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

Heitz D

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

Lynch M

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

Baker E

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

Little RD

9

1 reference

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19 September 2019

Wada M

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

language of work or name

English

0 references

publication date

1 September 1991

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

19 September 2019

published in

1 reference

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19 September 2019

volume

49

1 reference

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19 September 2019

issue

3

1 reference

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19 September 2019

page(s)

656-661

1 reference

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A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation

19 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Mitotic stability of yeast chromosomes: a colony color assay that measures nondisjunction and chromosome loss

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

A rodent-human hybrid containing Xq24-qter translocated to a hamster chromosome expresses the Xq27 folate-sensitive fragile site

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Cloning human telomeric DNA fragments into Saccharomyces cerevisiae using a yeast-artificial-chromosome vector

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Yeast artificial chromosomes containing human Xq24-Xq28 DNA: library construction and representation of probe sequences

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

An expanded mouse-human hybrid cell panel for mapping human chromosome 16.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Two progenitor cells for human oogonia inferred from pedigree data and the X-inactivation imprinting model of the fragile-X syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683130

Genomic Organization of Human Centromeric Alpha Satellite DNA: Characterization of a Chromosome 17 Alpha Satellite Sequence

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1882843

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1882843%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

PubMed publication ID

1882843

1 reference