(Q51001420)

26 March 2018

title

An Angelman syndrome clinic: report on 24 patients. (English)

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26 March 2018

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Leitner RP

1

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26 March 2018

Smith A

series ordinal

2

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26 March 2018

publication date

1 April 1996

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26 March 2018

Journal of Paediatrics and Child Health

published in

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26 March 2018

volume

32

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26 March 2018

issue

2

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26 March 2018

page(s)

94-98

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26 March 2018

Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

Is Angelman syndrome an alternate result of del(15)(q11q13)?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

The EEG in early diagnosis of the Angelman (happy puppet) syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

Diagnosis of Angelman syndrome in infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

Clinical research on Angelman syndrome in the United Kingdom: observations on 82 affected individuals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

Epilepsy in Angelman syndrome associated with chromosome 15q deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

Uniparental disomy, isodisomy, and imprinting: probable effects in man and strategies for their detection

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

Molecular and clinical study of 61 Angelman syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1754.1996.TB00902.X

10.1111/J.1440-1754.1996.TB00902.X

21 January 2018

Identifiers

DOI

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26 March 2018

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26 March 2018