(Q37376270)

20 August 2017

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title

Application of array-based comparative genome hybridization in children with developmental delay or mental retardation (English)

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20 August 2017

Jao-Shwann Liang

1

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20 August 2017

Keiko Shimojima

series ordinal

2

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20 August 2017

Toshiyuki Yamamoto

series ordinal

3

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20 August 2017

publication date

1 December 2008

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Pediatrics and neonatology

20 August 2017

published in

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20 August 2017

volume

49

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20 August 2017

issue

6

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20 August 2017

page(s)

213-217

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The epidemiology of mental retardation: challenges and opportunities in the new millennium

20 August 2017

cites work

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Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation

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7 January 2021

Medical applications of array CGH and the transformation of clinical cytogenetics

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7 January 2021

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

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7 January 2021

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

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7 January 2021

Oligonucleotide arrays for high-resolution analysis of copy number alteration in mental retardation/multiple congenital anomalies

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7 January 2021

Novel microdeletion syndromes detected by chromosome microarrays

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7 January 2021

Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness.

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The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

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7 January 2021

Subtle chromosomal rearrangements in children with unexplained mental retardation

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7 January 2021

American College of Medical Genetics guideline on the cytogenetic evaluation of the individual with developmental delay or mental retardation

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7 January 2021

A cytogeneticist's perspective on genomic microarrays

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7 January 2021

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

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7 January 2021

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

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7 January 2021

Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation

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7 January 2021

Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.

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7 January 2021

Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).

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7 January 2021

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation

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7 January 2021

Array comparative genomic hybridization in global developmental delay.

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7 January 2021

The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future

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7 January 2021

10.1016/S1875-9572(09)60013-9

Identifiers

DOI

1 reference

20 August 2017

1 reference