(Q48986959)

17 February 2018

title

Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method. (English)

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17 February 2018

Karine Poirier

6

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author name string

Yoann Saillour

1

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17 February 2018

Mireille Cossée

2

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17 February 2018

France Leturcq

3

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17 February 2018

Aurélie Vasson

4

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17 February 2018

Caroline Beugnet

5

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17 February 2018

Virginie Commere

7

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17 February 2018

Sébastien Sublemontier

8

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17 February 2018

Marion Viel

9

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17 February 2018

Franck Letourneur

10

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17 February 2018

Jean Claude Barbot

11

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17 February 2018

Nathalie Deburgrave

12

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17 February 2018

Jamel Chelly

13

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17 February 2018

Thierry Bienvenu

14

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17 February 2018

publication date

1 September 2008

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17 February 2018

published in

Human Mutation

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17 February 2018

volume

29

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17 February 2018

issue

9

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17 February 2018

page(s)

1083-1090

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17 February 2018

Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene

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1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Light-directed 5'-->3' synthesis of complex oligonucleotide microarrays

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

The detection of large deletions or duplications in genomic DNA.

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https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Simultaneous mutation scanning for gross deletions, duplications and point mutations in the DMD gene.

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https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Gross genomic rearrangements involving deletions in the CFTR gene: characterization of six new events from a large cohort of hitherto unidentified cystic fibrosis chromosomes and meta-analysis of the underlying mechanisms

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

A tiling resolution DNA microarray with complete coverage of the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Deletion and duplication screening in the DMD gene using MLPA.

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https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Rapid detection of CFTR gene rearrangements impacts on genetic counselling in cystic fibrosis

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https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

MLPA and MAPH: new techniques for detection of gene deletions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridization

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Duplications in the DMD gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20829

7 January 2021

Identifiers

DOI

10.1002/HUMU.20829

1 reference

17 February 2018

1 reference

17 February 2018