(Q40449967)

20 September 2017

title

Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis. (English)

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20 September 2017

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Björn Menten

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Frank Speleman

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20 September 2017

Joris R Vermeesch

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20 September 2017

Cindy Melotte

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20 September 2017

Guy Froyen

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20 September 2017

Steven Van Vooren

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20 September 2017

Binita Dutta

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20 September 2017

Nicole Maas

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20 September 2017

Stefan Vermeulen

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20 September 2017

Bart De Moor

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20 September 2017

Paul Van Hummelen

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20 September 2017

Peter Marynen

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20 September 2017

Jean-Pierre Fryns

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20 September 2017

Koen Devriendt

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20 September 2017

publication date

1 March 2005

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Journal of Histochemistry and Cytochemistry

20 September 2017

published in

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20 September 2017

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20 September 2017

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20 September 2017

page(s)

413-422

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

20 September 2017

cites work

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

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The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

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Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation

21 January 2018

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

21 January 2018

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Subtle chromosomal rearrangements in children with unexplained mental retardation

21 January 2018

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Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

21 January 2018

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"Molecular rulers" for calibrating phenotypic effects of telomere imbalance

21 January 2018

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

21 January 2018

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Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.

21 January 2018

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Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations.

21 January 2018

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Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages

21 January 2018

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The performance of CGH array for the detection of cryptic constitutional chromosome imbalances

21 January 2018

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Large-scale copy number polymorphism in the human genome

21 January 2018

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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

21 January 2018

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

21 January 2018

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Automated array-based genomic profiling in chronic lymphocytic leukemia: development of a clinical tool and discovery of recurrent genomic alterations

21 January 2018

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Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map.

21 January 2018

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https://api.crossref.org/works/10.1369%2FJHC.4A6436.2005

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1369%2FJHC.4A6436.2005

21 January 2018

Identifiers

DOI

10.1369/JHC.4A6436.2005

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20 September 2017

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