(Q41048598)

26 September 2017

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

1 reference

Adrianus Henricus Maria Geurts van Kessel

26 September 2017

10

object named as

Ad Geurts van Kessel

0 references

Joris A Veltman

object named as

Joris A Veltman

1

0 references

Han G. Brunner

8

object named as

Han G Brunner

1 reference

26 September 2017

Eric F P M Schoenmakers

2

1 reference

26 September 2017

Bert H Eussen

3

1 reference

26 September 2017

Irene Janssen

4

1 reference

26 September 2017

Gerard Merkx

5

1 reference

26 September 2017

Brigitte van Cleef

6

1 reference

26 September 2017

Conny M van Ravenswaaij

7

1 reference

26 September 2017

Dominique Smeets

9

1 reference

26 September 2017

Ad Geurts van Kessel

10

1 reference

26 September 2017

language of work or name

English

0 references

publication date

9 April 2002

1 reference

American Journal of Human Genetics

26 September 2017

1 reference

26 September 2017

70

1 reference

26 September 2017

5

1 reference

26 September 2017

1269-1276

1 reference

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Clinical studies on submicroscopic subtelomeric rearrangements: a checklist

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Williams syndrome: from genotype through to the cognitive phenotype

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Prader-Willi and Angelman syndromes: sister imprinted disorders

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Comparative genomic hybridization: uses and limitations

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

The 22q11 deletion syndromes

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Comparative genomic hybridisation

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Measurement of locus copy number by hybridisation with amplifiable probes

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Subtle chromosomal rearrangements in children with unexplained mental retardation

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Use of primed in situ labeling (PRINS) for the detection of telomeric deletions associated with mental retardation

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

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

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL)

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

2 December 2018

BACking up the promises

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447601

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

2 December 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Wolf-Hirschhorn syndrome and Pitt-Rogers-Danks syndrome

1 reference

12 December 2020

A novel chromosomal region of allelic loss, 4q32-q34, in human osteosarcomas revealed by representational difference analysis

1 reference

12 December 2020

Identifiers

DOI

10.1086/340426

1 reference

26 September 2017

1 reference

26 September 2017

PubMed publication ID

11951177

1 reference