(Q51590622)

7 April 2018

title

Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos. (English)

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7 April 2018

11

Thomas D'Hooghe

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7 April 2018

Thierry Voet

1

object named as

Thierry Voet

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7 April 2018

Joris R Vermeesch

12

object named as

Joris R Vermeesch

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7 April 2018

Yves Moreau

10

object named as

Yves Moreau

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7 April 2018

author name string

Evelyne Vanneste

2

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7 April 2018

Niels Van der Aa

3

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7 April 2018

Cindy Melotte

4

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7 April 2018

Sigrun Jackmaert

5

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7 April 2018

Tamara Vandendael

6

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7 April 2018

Matthias Declercq

7

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7 April 2018

Sophie Debrock

8

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7 April 2018

Jean-Pierre Fryns

9

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7 April 2018

publication date

1 July 2011

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7 April 2018

published in

Human Mutation

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7 April 2018

volume

32

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7 April 2018

issue

7

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7 April 2018

page(s)

783-793

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7 April 2018

On the possible origins of DNA damage in human spermatozoa.

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Biological and clinical significance of DNA damage in the male germ line.

21 January 2018

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Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions

21 January 2018

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Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution

21 January 2018

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Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

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Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis

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The origins, patterns and implications of human spontaneous mutation

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Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH.

21 January 2018

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Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays.

21 January 2018

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Preclinical validation of a microarray method for full molecular karyotyping of blastomeres in a 24-h protocol

21 January 2018

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Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements

21 January 2018

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Paternal contributions: new functional insights for spermatozoal RNA

21 January 2018

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Conception to ongoing pregnancy: the 'black box' of early pregnancy loss

21 January 2018

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Checkpoint-apoptosis uncoupling in human and mouse embryonic stem cells: a source of karyotpic instability

21 January 2018

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Early embryonic chromosome instability results in stable mosaic pattern in human tissues

21 January 2018

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A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

21 January 2018

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Reproductive biology: delivering spermatozoan RNA to the oocyte.

21 January 2018

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Centric fission--simple and complex mechanisms.

21 January 2018

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Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome

21 January 2018

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Whole-genome multiple displacement amplification from single cells

21 January 2018

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Proliferation of aneuploid human cells is limited by a p53-dependent mechanism.

21 January 2018

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Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays

21 January 2018

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Chromosome instability is common in human cleavage-stage embryos.

21 January 2018

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Chromosome abnormalities identified by comparative genomic hybridization in embryos from women with repeated implantation failure.

21 January 2018

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Are tests of sperm DNA damage clinically useful? Pros and cons

21 January 2018

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Inverted duplications deletions: underdiagnosed rearrangements??

21 January 2018

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Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndrome

21 January 2018

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Human gene expression first occurs between the four- and eight-cell stages of preimplantation development

21 January 2018

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Preferential loss of the paternal alleles in the 18q- syndrome

21 January 2018

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7 January 2021

Motile human normozoospermic and oligozoospermic semen samples show a difference in double-strand DNA break incidence

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https://api.crossref.org/works/10.1002%2FHUMU.21502

7 January 2021

Successful pregnancies after application of array-comparative genomic hybridization in PGS-aneuploidy screening

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https://api.crossref.org/works/10.1002%2FHUMU.21502

7 January 2021

Preimplantation genetic diagnosis for an insertional translocation carrier

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https://api.crossref.org/works/10.1002%2FHUMU.21502

7 January 2021

Parental origin of chromosome 5 deletions in the cri-du-chat syndrome

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https://api.crossref.org/works/10.1002%2FHUMU.21502

7 January 2021

Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation

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https://api.crossref.org/works/10.1002%2FHUMU.21502

7 January 2021

Molecular characterization of a new patient with a non-recurrent inv dup del 2q and review of the mechanisms for this rearrangement

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https://api.crossref.org/works/10.1002%2FHUMU.21502

7 January 2021

Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization

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https://api.crossref.org/works/10.1002%2FHUMU.21502

7 January 2021

Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridization

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https://api.crossref.org/works/10.1002%2FHUMU.21502

7 January 2021

Identifiers

DOI

10.1002/HUMU.21502

1 reference

7 April 2018

1 reference

7 April 2018