(Q33905292)

29 July 2017

title

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

1 reference

Adrianus Henricus Maria Geurts van Kessel

29 July 2017

author

object named as

Ad Geurts van Kessel

0 references

Joris A Veltman

0 references

Han G Brunner

1 reference

29 July 2017

Bert B A de Vries

1 reference

29 July 2017

Irene M Janssen

1 reference

29 July 2017

Ad Geurts van Kessel

1 reference

29 July 2017

Lisenka E L M Vissers

1 reference

29 July 2017

Kazutoyo Osoegawa

1 reference

29 July 2017

Ton Feuth

1 reference

29 July 2017

Chik On Choy

1 reference

29 July 2017

Huub Straatman

1 reference

29 July 2017

Walter van der Vliet

1 reference

29 July 2017

Erik H L P G Huys

1 reference

29 July 2017

Anke van Rijk

1 reference

29 July 2017

Dominique Smeets

1 reference

29 July 2017

Conny M A van Ravenswaaij-Arts

1 reference

29 July 2017

Nine V Knoers

1 reference

29 July 2017

Ineke van der Burgt

1 reference

29 July 2017

Pieter J de Jong

1 reference

29 July 2017

Eric F P M Schoenmakers

1 reference

29 July 2017

language of work or name

English

0 references

publication date

18 November 2003

1 reference

American Journal of Human Genetics

29 July 2017

published in

1 reference

29 July 2017

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29 July 2017

1 reference

29 July 2017

page(s)

1261-1270

1 reference

12p-amplicon structure analysis in testicular germ cell tumors of adolescents and adults by array CGH.

29 July 2017

cites work

1 reference

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5 July 2018

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Telomeres: a diagnosis at the end of the chromosomes

5 July 2018

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Mutational mechanisms of Williams-Beuren syndrome deletions

5 July 2018

1 reference

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5 July 2018

Mowat-Wilson syndrome

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects

5 July 2018

1 reference

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Segmental polymorphisms in the proterminal regions of a subset of human chromosomes

5 July 2018

1 reference

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Cardiovascular manifestations in 75 patients with Williams syndrome

5 July 2018

1 reference

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Transcriptional activity of multiple copies of a subtelomerically located olfactory receptor gene that is polymorphic in number and location

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Assembly of microarrays for genome-wide measurement of DNA copy number

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Mapping and characterization of the mouse and human SS18 genes, two human SS18-like genes and a mouse Ss18 pseudogene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Clinical studies on submicroscopic subtelomeric rearrangements: a checklist

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

A bacterial artificial chromosome library for sequencing the complete human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Duplication of chromosome region 8p23.1-->p23.3: a benign variant?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Subtle chromosomal rearrangements in children with unexplained mental retardation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Interstitial 7q deletion [46,XY,del (7) (pter----cen::q112----qter)] in a retarded quadriplegic boy with normal beta glucuronidase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Expressed hypervariable polymorphism of apolipoprotein (a).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Hidden gene amplifications in aggressive B-cell non-Hodgkin lymphomas detected by microarray-based comparative genomic hybridization.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Integration of cytogenetic landmarks into the draft sequence of the human genome

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

The promise and pitfalls of telomere region-specific probes

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

A case of Williams syndrome with a large, visible cytogenetic deletion.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

Molecular definition of the extreme size polymorphism in apolipoprotein(a).

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180392

The end of the beginning of chromosome ends

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14628292

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14628292

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/379977

1 reference

29 July 2017

1 reference

29 July 2017

1 reference