(Q37988561)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22369279%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

title

Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22369279%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

0 references

0 references

Evica Rajcan-Separovic

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22369279%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

Elena Lopez-Rangel

4

1 reference

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24 January 2020

author name string

Y Qiao

1

1 reference

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24 January 2020

C Tyson

2

1 reference

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24 January 2020

M Hrynchak

3

1 reference

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24 January 2020

J Hildebrand

5

1 reference

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24 January 2020

S Martell

6

1 reference

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24 January 2020

C Fawcett

7

1 reference

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24 January 2020

L Kasmara

8

1 reference

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24 January 2020

K Calli

9

1 reference

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24 January 2020

C Harvard

10

1 reference

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24 January 2020

X Liu

11

1 reference

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24 January 2020

J J A Holden

12

1 reference

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24 January 2020

S M E Lewis

13

1 reference

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24 January 2020

publication date

9 April 2012

1 reference

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24 January 2020

1 reference

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24 January 2020

volume

83

1 reference

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24 January 2020

issue

2

1 reference

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24 January 2020

page(s)

145-154

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22369279%20AND%20SRC:MED&resulttype=core&format=json

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects

24 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

Functional impact of global rare copy number variation in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

Molecular karyotyping using an SNP array for genomewide genotyping.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

Copy number variation in the genome; the human DMD gene as an example

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2012.01860.X

10.1111/J.1399-0004.2012.01860.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22369279%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

1 reference