(Q50312781)

2 March 2018

title

The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findings. (English)

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2 March 2018

main subject

electroencephalography

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S Buoni

1

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2 March 2018

L Sorrentino

2

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2 March 2018

M A Farnetani

3

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2 March 2018

L Pucci

4

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2 March 2018

A Fois

5

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2 March 2018

publication date

1 June 2000

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2 March 2018

Journal of Child Neurology

published in

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2 March 2018

volume

15

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2 March 2018

issue

6

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2 March 2018

page(s)

380-385

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2 March 2018

Angelman syndrome in three siblings: characteristic epileptic seizures and EEG abnormalities

cites work

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500605

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500605

Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500605

A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500605

Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500605

The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500605

Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500605

Maternal origin of inv dup(15) chromosomes in infantile autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500605

UBE3A/E6-AP mutations cause Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500605

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500605

10.1177/088307380001500605

21 January 2018

Identifiers

DOI

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2 March 2018

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2 March 2018