(Q38491381)

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Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes.

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11715006%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11715006%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

Marsha D Speevak

3

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3 December 2019

author name string

Y S Fan

1

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3 December 2019

Y Zhang

2

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11715006%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

S Farrell

4

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3 December 2019

J H Jung

5

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3 December 2019

V M Siu

6

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3 December 2019

language of work or name

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publication date

1 November 2001

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3 December 2019

Genetics in Medicine

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3 December 2019

3

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3 December 2019

6

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3 December 2019

416-421

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3 December 2019

describes a project that uses

fluorescence in situ hybridization

1 reference

based on heuristic

inferred from title

https://scigraph.springernature.com/pub.10.1097/00125817-200111000-00007

0 references

Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

The highest gene concentrations in the human genome are in telomeric bands of metaphase chromosomes

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Two 22q telomere deletions serendipitously detected by FISH

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Familial cryptic (20;21) translocation identified by in situ hybridization technologies.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

An optimized set of human telomere clones for studying telomere integrity and architecture.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Subtle chromosomal rearrangements in children with unexplained mental retardation

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

The promise and pitfalls of telomere region-specific probes

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Sequence organization of the human chromosome 2q telomere.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Clinical studies on submicroscopic subtelomeric rearrangements: a checklist

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalities

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Reply to Horvath et al

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangements

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200111000-00007

21 January 2018

Identifiers

10.1097/00125817-200111000-00007

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11715006%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

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1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11715006%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

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