(Q33760683)

29 July 2017

1 reference

title

Angelman syndrome: a review of clinical and genetic aspects (English)

1 reference

29 July 2017

1 reference

Laan LA

1

1 reference

PubMed ID

10536901

29 July 2017

v Haeringen A

series ordinal

2

1 reference

PubMed ID

10536901

29 July 2017

Brouwer OF

series ordinal

3

1 reference

29 July 2017

1 September 1999

1 reference

Clinical Neurology and Neurosurgery

29 July 2017

1 reference

29 July 2017

101

1 reference

29 July 2017

161-170

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29 July 2017

3

1 reference

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

29 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Clinical, cytogenetic, and molecular diagnosis of Angelman syndrome: estimated prevalence rate in a Danish county.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

‘Puppet’ Children A Report on Three Cases

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Angelman syndrome: clinical profile

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

The "happy puppet" syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

The Angelman ("happy puppet") syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Diagnosis of Angelman syndrome in infants

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Clinical profile of Angelman syndrome at different ages

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Angelman syndrome in adulthood

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Manifestations in institutionalised adults with Angelman syndrome due to deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

The Angelman or "happy puppet" syndrome. Clinical and electroencephalographic features and cerebral blood flow.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Seizure and EEG patterns in Angelman's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Evolution of epilepsy and EEG findings in Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Epilepsy in Angelman syndrome associated with chromosome 15q deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Angelman's syndrome: clinical and electroencephalographic findings.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Angelman's syndrome: a neuropathological study.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

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%2FS0303-8467%2899%2900030-X

7 January 2021

The association of Angelman's syndrome with deletions within 15q11-13

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

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%2FS0303-8467%2899%2900030-X

7 January 2021

Uniparental paternal disomy in Angelman's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Molecular study of chromosome 15 in 22 patients with Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Imprinting makes an impression

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

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%2FS0303-8467%2899%2900030-X

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%2FS0303-8467%2899%2900030-X

7 January 2021

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%2FS0303-8467%2899%2900030-X

7 January 2021

DNA deletion and its parental origin in Angelman syndrome patients

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Paternal uniparental disomy of chromosome 15 in a child with Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Uniparental disomies in unselected populations

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

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%2FS0303-8467%2899%2900030-X

7 January 2021

Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Mutation analysis of UBE3A in Angelman syndrome patients

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

1 reference

7 January 2021

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

1 reference

7 January 2021

Communication development in Angelman's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2899%2900030-X

7 January 2021

10.1016/S0303-8467(99)00030-X

Identifiers

DOI

1 reference

29 July 2017

1 reference

PubMed ID

10536901