(Q46455433)

22 December 2017

title

Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array (English)

1 reference

22 December 2017

author

Magnus Nordenskjöld

15

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22 December 2017

Jan Dumański

19

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22 December 2017

Ann-Charlotte Thuresson

Ann-Charlotte Thuresson

8

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Robin Andersson

Robin Andersson

5

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Arkadiusz Piotrowski

Arkadiusz Piotrowski

3

0 references

Caisa M Hansson

11

Caisa M Hansson

1 reference

22 December 2017

Helena Nord-Ljungquist

4

Helena Nord

1 reference

22 December 2017

Bogdan Adam Michalski

7

Adam Bogdan

1 reference

22 December 2017

Johanna Sandgren

2

Johanna Sandgren

1 reference

22 December 2017

Jan Komorowski

17

Jan Komorowski

1 reference

22 December 2017

Teresita Díaz de Ståhl

1

Teresita Díaz de Ståhl

1 reference

22 December 2017

Desiree von Tell

10

Desiree von Tell

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22 December 2017

author name string

Uwe Menzel

6

1 reference

22 December 2017

Andrzej Poplawski

9

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22 December 2017

Amir I Elshafie

12

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22 December 2017

Gehad Elghazali

13

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22 December 2017

Stephan Imreh

14

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22 December 2017

Meena Upadhyaya

16

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22 December 2017

Carl E G Bruder

18

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22 December 2017

publication date

1 March 2008

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22 December 2017

published in

Human Mutation

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22 December 2017

volume

29

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22 December 2017

page(s)

398-408

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22 December 2017

issue

3

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22 December 2017

cites work

The LCB Data Warehouse

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Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22.

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The human-specific Yp11.2/Xq21.3 homology block encodes a potentially functional testis-specific TGIF-like retroposon.

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2.

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

A high-resolution survey of deletion polymorphism in the human genome

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH.

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Accurate and reliable high-throughput detection of copy number variation in the human genome

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Detection of large-scale variation in the human genome

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Global variation in copy number in the human genome

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Human genome sequence variation and the influence of gene history, mutation and recombination

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Large-scale copy number polymorphism in the human genome

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Segmental duplications and copy-number variation in the human genome

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Detecting copy number variation in the human genome using comparative genomic hybridization

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https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Fine-scale structural variation of the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20659

7 January 2021

Identifiers

DOI

10.1002/HUMU.20659

1 reference

22 December 2017

PubMed ID

18058796

1 reference

22 December 2017