(Q51888410)

17 April 2018

title

Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations. (English)

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17 April 2018

author name string

Diane L Pickering

1

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17 April 2018

James D Eudy

2

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17 April 2018

Ann Haskins Olney

3

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17 April 2018

Bhavana J Dave

4

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17 April 2018

Denae Golden

5

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17 April 2018

Jadd Stevens

6

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17 April 2018

Warren G Sanger

7

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17 April 2018

language of work or name

English

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publication date

1 April 2008

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17 April 2018

published in

Genetics in Medicine

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17 April 2018

volume

10

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17 April 2018

issue

4

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17 April 2018

page(s)

262-266

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17 April 2018

https://scigraph.springernature.com/pub.10.1097/gim.0b013e31816b64ad

exact match

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cites work

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Practice parameter: evaluation of the child with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and The Practice Committee of the Child Neurology Society.

21 January 2018

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Diagnostic evaluation of developmental delay/mental retardation: An overview

21 January 2018

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Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities

21 January 2018

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Microarray-based comparative genomic hybridization and its applications in human genetics

21 January 2018

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Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E31816B64AD

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31816B64AD

Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E31816B64AD

Genomic disorders on 22q11

21 January 2018

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Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

21 January 2018

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Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature review

21 January 2018

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Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

21 January 2018

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A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome

21 January 2018

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Molecular epigenetics of Angelman syndrome

21 January 2018

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Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

21 January 2018

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10.1097/GIM.0B013E31816B64AD

21 January 2018

Identifiers

DOI

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17 April 2018

Dimensions Publication ID

1052316491

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17 April 2018