(Q51912968)

English

Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies.

scientific article published in January 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies. (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

Bernard Thienpont

1

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

author name string

Gewillig M

2

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

Fryns JP

3

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

Devriendt K

4

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

Vermeesch J

5

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

publication date

1 January 2006

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

Cytogenetics and Genome Research

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

114

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Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

3-4

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

338-341

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

Dynamics of DNA double-strand breaks revealed by clustering of damaged chromosome domains.

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

Diagnostic genome profiling in mental retardation

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injection

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

Array CGH detection of a cryptic deletion in a complex chromosome rearrangement.

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

Nonhomologous recombination in mammalian cells: role for short sequence homologies in the joining reaction

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

Molecular cytogenetic characterization of multiple intrachromosomal rearrangements of chromosome 2q in a patient with Waardenburg's syndrome and other congenital defects

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

The new cytogenetics: blurring the boundaries with molecular biology

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

Molecular cytogenetic characterization of a familial der(1)del(1)(p36.33)dup(1)(p36.33p36.22) with variable phenotype.

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

Ten years follow up of a boy with a complex chromosomal rearrangement: going from a > 5 to 15-breakpoint CCR

1 reference

https://api.crossref.org/works/10.1159%2F000094223

21 January 2018

Identifiers

10.1159/000094223

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/16954676

ResearchGate publication ID

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