(Q24675632)

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Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15060094%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15060094%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

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learning disability

1 reference

based on heuristic

inferred from title

4

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Europe PubMed Central

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26 December 2019

Damien Sanlaville

8

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Europe PubMed Central

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26 December 2019

Laurence Colleaux

10

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26 December 2019

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C Shaw-Smith

1

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26 December 2019

R Redon

2

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26 December 2019

L Rickman

3

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26 December 2019

L Willatt

5

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26 December 2019

H Fiegler

6

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26 December 2019

H Firth

7

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26 December 2019

R Winter

9

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Europe PubMed Central

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26 December 2019

M Bobrow

11

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Europe PubMed Central

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26 December 2019

N P Carter

12

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Europe PubMed Central

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26 December 2019

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1 April 2004

1 reference

Europe PubMed Central

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26 December 2019

Journal of Medical Genetics

1 reference

Europe PubMed Central

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26 December 2019

41

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Europe PubMed Central

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26 December 2019

4

1 reference

Europe PubMed Central

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26 December 2019

241-248

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15060094%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

7 April 2017

The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

7 April 2017

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

Genomic microarrays in human genetic disease and cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

Telomeres: a diagnosis at the end of the chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

High-resolution analysis of paraffin-embedded and formalin-fixed prostate tumors using comparative genomic hybridization to genomic microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

High-resolution genomic profiling of occult micrometastatic tumor cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

Fully automatic quantification of microarray image data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

Interstitial deletion 1p in a 30 year old woman.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

A presumptive translocation 1p;2q resulting in duplication 1p and deletion 2q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

De novo interstitial deletion del(1)(p21p32)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 September 2017

Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

30 May 2018

Additional case of de novo interstitial deletion del(17)(q21.3q23) and expansion of the phenotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

30 May 2018

Two cases of interstitial deletion 1p

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

30 May 2018

Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 November 2018

A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 November 2018

Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 November 2018

Array-based comparative genomic hybridization for the differential diagnosis of renal cell cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 November 2018

Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 November 2018

High resolution comparative genomic hybridisation in clinical cytogenetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735726

28 November 2018

A unique de novo interstitial deletion del(17) (q21.3q23) in a phenotypically abnormal infant

1 reference

https://pubmed.ncbi.nlm.nih.gov/15060094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions within chromosome 22q11 in familial congenital heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15060094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15q

1 reference

https://pubmed.ncbi.nlm.nih.gov/15060094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH

1 reference

https://pubmed.ncbi.nlm.nih.gov/15060094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The end of the beginning of chromosome ends

1 reference

https://pubmed.ncbi.nlm.nih.gov/15060094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/15060094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence genotyping for screening cryptic telomeric rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/15060094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.2003.017731

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15060094%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15060094%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15060094%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

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