(Q41927444)

14 October 2017

title

Angelman syndrome assessed by neurological and molecular cytogenetic investigations (English)

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14 October 2017

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Hou JW

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14 October 2017

Wang PJ

series ordinal

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14 October 2017

Wang TR

series ordinal

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14 October 2017

publication date

1 January 1997

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14 October 2017

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14 October 2017

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14 October 2017

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14 October 2017

page(s)

17-22

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‘Puppet’ Children A Report on Three Cases

14 October 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Clinical profile of Angelman syndrome at different ages

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Characterization of a methylation imprint in the Prader-Willi syndrome chromosome region

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Precocious puberty in a case with probable Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

On the prevalence of Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Exclusion of the GABAA-receptor beta 3 subunit gene as the Angelman's syndrome gene

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Diagnosis of Angelman syndrome in infants

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Diagnosis in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

Angelman syndrome and vermian cyst

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900264-0

7 January 2021

10.1016/S0887-8994(96)00264-0

Identifiers

DOI

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14 October 2017

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