Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome. (Q55117910)

21 June 2018

title

Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome. (English)

1 reference

21 June 2018

author name string

Merlin G Butler

1

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21 June 2018

William Fischer

2

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21 June 2018

Nataliya Kibiryeva

3

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21 June 2018

Douglas C Bittel

4

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21 June 2018

language of work or name

English

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publication date

1 April 2008

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21 June 2018

American Journal of Medical Genetics

published in

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21 June 2018

volume

146A

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21 June 2018

issue

7

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21 June 2018

page(s)

854-860

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21 June 2018

Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities

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22 June 2018

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Strong association of de novo copy number mutations with autism

22 June 2018

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

22 June 2018

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22 June 2018

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22 June 2018

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22 June 2018

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Genome assembly comparison identifies structural variants in the human genome.

22 June 2018

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Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome

22 June 2018

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22 June 2018

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Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology

22 June 2018

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22 June 2018

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22 June 2018

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High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage

22 June 2018

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

22 June 2018

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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

22 June 2018

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Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

22 June 2018

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Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements

22 June 2018

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Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.

22 June 2018

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Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human

22 June 2018

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

22 June 2018

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

22 June 2018

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Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers

22 June 2018

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Whole genome microarray analysis of gene expression in Prader-Willi syndrome.

22 June 2018

1 reference

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Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5438264

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

13 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18266248

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18266248

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/AJMG.A.32249

1 reference

21 June 2018

PMCID

5438264

1 reference

21 June 2018

PubMed ID

18266248

1 reference

21 June 2018