Autistic disorder and 22q11.2 duplication. (Q50313803)

2 March 2018

title

Autistic disorder and 22q11.2 duplication. (English)

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2 March 2018

main subject

autism

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author name string

Nahit Motavalli Mukaddes

series ordinal

1

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2 March 2018

Sabri Herguner

series ordinal

2

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2 March 2018

publication date

1 January 2007

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2 March 2018

World Journal of Biological Psychiatry

published in

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2 March 2018

volume

8

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2 March 2018

issue

2

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2 March 2018

page(s)

127-130

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2 March 2018

Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome

cites work

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

A common molecular basis for rearrangement disorders on chromosome 22q11

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

On the significance of linkage studies of complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

On cognitive variability in velocardiofacial syndrome: profound mental retardation and autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

Microduplication and triplication of 22q11.2: a highly variable syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15622970601026701

10.1080/15622970601026701

21 January 2018

Identifiers

DOI

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2 March 2018

PubMed ID

17455106

1 reference

2 March 2018