(Q51907423)

English

Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment.

scientific article published in January 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment. (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

neurological disorder

1 reference

based on heuristic

inferred from title

author name string

Murthy SK

1

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

Nygren AO

2

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

El Shakankiry HM

3

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

Schouten JP

4

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

Al Khayat AI

5

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

Ridha A

6

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

Al Ali MT

7

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

publication date

1 January 2007

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

Cytogenetics and Genome Research

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

116

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

1-2

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

135-140

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Recent segmental duplications in the human genome

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Identification of Four Highly Conserved Genes between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transposition Mediated by Flanking Duplicons

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Clinical studies on submicroscopic subtelomeric rearrangements: a checklist

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Subtle chromosomal rearrangements in children with unexplained mental retardation

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Genomic imbalances in mental retardation

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects.

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities

1 reference

https://api.crossref.org/works/10.1159%2F000097433

21 January 2018

Identifiers

10.1159/000097433

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 April 2018

http://europepmc.org/abstract/MED/17268193

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