(Q46252280)

20 December 2017

title

Variation of CNV distribution in five different ethnic populations (English)

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20 December 2017

author

Lisenka Vissers

2

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20 December 2017

Esther van de Vosse

8

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20 December 2017

author name string

White SJ

1

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20 December 2017

Geurts van Kessel A

3

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20 December 2017

de Menezes RX

4

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20 December 2017

Kalay E

5

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20 December 2017

Lehesjoki AE

6

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20 December 2017

Giordano PC

7

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20 December 2017

Breuning MH

9

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20 December 2017

Brunner HG

10

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20 December 2017

den Dunnen JT

11

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20 December 2017

Veltman JA

12

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20 December 2017

publication date

1 January 2007

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20 December 2017

Cytogenetics and Genome Research

published in

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20 December 2017

volume

118

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20 December 2017

issue

1

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20 December 2017

page(s)

19-30

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20 December 2017

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

cites work

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Segmental duplications: organization and impact within the current human genome project assembly

21 January 2018

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Association of an extended haplotype in the tau gene with progressive supranuclear palsy

21 January 2018

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Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

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A worldwide survey of haplotype variation and linkage disequilibrium in the human genome

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Diagnostic genome profiling in mental retardation

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The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

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Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster

21 January 2018

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Detection of large-scale variation in the human genome

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Molecular mechanisms for genomic disorders

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A haplotype map of the human genome

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Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).

21 January 2018

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A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.

21 January 2018

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Common deletion polymorphisms in the human genome.

21 January 2018

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Comparative genomic hybridization

21 January 2018

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Global variation in copy number in the human genome

21 January 2018

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Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics.

21 January 2018

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

21 January 2018

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Large-scale copy number polymorphism in the human genome

21 January 2018

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Segmental duplications and copy-number variation in the human genome

21 January 2018

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Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

21 January 2018

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Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

21 January 2018

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Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

21 January 2018

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A common inversion under selection in Europeans

21 January 2018

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Fine-scale structural variation of the human genome

21 January 2018

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FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

21 January 2018

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Human diallelic insertion/deletion polymorphisms

21 January 2018

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Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

21 January 2018

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Identification of frequent chromosome copy-number polymorphisms by use of high-resolution single-nucleotide-polymorphism arrays

21 January 2018

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Analysis of the DNA sequence and duplication history of human chromosome 15

21 January 2018

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Common deletions and SNPs are in linkage disequilibrium in the human genome

21 January 2018

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21 January 2018

Identifiers

DOI

10.1159/000106437

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20 December 2017

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20 December 2017