(Q35433098)

8 August 2017

title

Applications of comparative genomic hybridisation in constitutional chromosome studies (English)

1 reference

8 August 2017

Breen CJ

1

1 reference

8 August 2017

Barton L

2

1 reference

8 August 2017

Carey A

3

1 reference

8 August 2017

Dunlop A

4

1 reference

8 August 2017

Glancy M

5

1 reference

8 August 2017

Hall K

6

1 reference

8 August 2017

Hegarty AM

7

1 reference

8 August 2017

Khokhar MT

8

1 reference

8 August 2017

Power M

9

1 reference

8 August 2017

Ryan K

10

1 reference

8 August 2017

Green AJ

11

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8 August 2017

Stallings RL

12

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8 August 2017

language of work or name

English

0 references

publication date

1 July 1999

1 reference

Journal of Medical Genetics

8 August 2017

published in

1 reference

8 August 2017

volume

36

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8 August 2017

issue

7

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8 August 2017

page(s)

511-517

1 reference

Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

Genome screening by comparative genomic hybridization

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

Karyotyping human chromosomes by combinatorial multi-fluor FISH.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

Comparative genomic hybridization in clinical cytogenetics

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

Peters' anomaly associated with partial deletion of the long arm of chromosome 11.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734415

Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridization

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10424810

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1734415

1 reference

8 August 2017

1 reference