(Q40923007)

English

Angelman syndrome

scientific article published on August 1995

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scholarly article

1 reference

Europe PubMed Central

24 September 2017

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Europe PubMed Central

Angelman syndrome (English)

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Europe PubMed Central

24 September 2017

author name string

Williams CA

1

1 reference

Europe PubMed Central

24 September 2017

Zori RT

2

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Europe PubMed Central

24 September 2017

Hendrickson J

3

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Europe PubMed Central

24 September 2017

Stalker H

4

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Europe PubMed Central

24 September 2017

Marum T

5

1 reference

Europe PubMed Central

24 September 2017

Whidden E

6

1 reference

Europe PubMed Central

24 September 2017

Driscoll DJ

7

1 reference

Europe PubMed Central

24 September 2017

publication date

1 August 1995

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Europe PubMed Central

24 September 2017

Current problems in pediatrics

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Europe PubMed Central

24 September 2017

25

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Europe PubMed Central

24 September 2017

7

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Europe PubMed Central

24 September 2017

216-231

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Europe PubMed Central

24 September 2017

‘Puppet’ Children A Report on Three Cases

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The "happy puppet" syndrome

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https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

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The “Happy Puppet” Syndrome: Two New Cases and a Review of Five Previous Cases

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Fourteen Happy Puppets

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https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

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The Angelman syndrome in two brothers.

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The Angelman ("happy puppet") syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

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Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular and clinical study of 61 Angelman syndrome patients

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Angelman syndrome: clinical profile

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular mechanisms in Angelman syndrome: a survey of 93 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical profile of Angelman syndrome at different ages

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

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Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletions of proximal 15q without Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular study of chromosome 15 in 22 patients with Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The p locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

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Tissue-specific expression and cDNA cloning of small nuclear ribonucleoprotein-associated polypeptide N.

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional imprinting and epigenetic modification of the human SNRPN gene

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Uniparental paternal disomy in Angelman's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

DNA deletion and its parental origin in Angelman syndrome patients

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

X linked mental retardation with non-deletional alpha thalassaemia (ATR-X): further delineation of the phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Diagnosis of Angelman syndrome in infants

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation.

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Hypopigmentation in Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Angelman's syndrome in the first year of life

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Angelman syndrome and vermian cyst

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Puppet-like syndrome of Angelman: a pathologic and neurochemical study

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Angelman and Prader-Willi syndrome: a magnetic resonance imaging study of differences in cerebral structure.

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Angelman ("happy puppet") syndrome--seven new cases documented by cerebral computed tomography: review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Communication, cognition, and social interaction in the Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Laughter in epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

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Gelastic Epilepsy. Onset in neonatal period

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Normal and pathologic laughter in children

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Recurrence risk in the Angelman ("happy puppet") syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Alpha-fetoprotein in Angelman Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic imprinting in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS0045-9380%2806%2980036-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0045-9380(06)80036-8

1 reference

Europe PubMed Central

24 September 2017

1 reference

Europe PubMed Central

24 September 2017

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