(Q50302516)

2 March 2018

title

Array Comparative Genomic Hybridization Findings in a Cohort Referred for an Autism Evaluation (English)

1 reference

https://api.crossref.org/works/10.1177/0883073810370479

20 June 2024

0 references

Lois Starr

2

1 reference

2 March 2018

Dianne Pickering

3

1 reference

2 March 2018

Gwenn Skar

4

1 reference

2 March 2018

Kristi Dehaai

5

1 reference

2 March 2018

G. Bradley Schaefer

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20729506

20 June 2024

Warren G. Sanger

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20729506

20 June 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20729506

20 June 2024

publication date

20 August 2010

1 reference

2 March 2018

full work available at URL

http://journals.sagepub.com/doi/pdf/10.1177/0883073810370479

1 reference

https://api.crossref.org/works/10.1177/0883073810370479

Journal of Child Neurology

20 June 2024

published in

1 reference

2 March 2018

volume

25

1 reference

2 March 2018

issue

12

1 reference

2 March 2018

page(s)

1498-1503

1 reference

2 March 2018

Autism spectrum disorders: molecular genetic advances

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Clinical genetics evaluation in identifying the etiology of autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

The diagnostic utility of a genetics evaluation in children with pervasive developmental disorders

21 January 2018

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https://api.crossref.org/works/10.1177%2F0883073810370479

Diagnostic evaluation of developmental delay/mental retardation: An overview

21 January 2018

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https://api.crossref.org/works/10.1177%2F0883073810370479

The yield of the medical evaluation of children with pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Outcomes of genetic evaluation in children with pervasive developmental disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Etiologic yield of autistic spectrum disorders: a prospective study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Genetic testing in autism: how much is enough?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Association between microdeletion and microduplication at 16p11.2 and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Genetic studies in autistic disorder and chromosome 15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Intrachromosomal triplication of 15q11-q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

CCG repeats in cDNAs from human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Analysis of the neuroligin 4Y gene in patients with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Analysis of four neuroligin genes as candidates for autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Recurrent 16p11.2 microdeletions in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810370479

Essential versus complex autism: definition of fundamental prognostic subtypes

21 January 2018

7

1 reference

https://api.crossref.org/works/10.1177/0883073810370479

Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia.

20 June 2024

26

1 reference

https://api.crossref.org/works/10.1177/0883073810370479

20 June 2024

Identifiers

1 reference

2 March 2018

1 reference

2 March 2018