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Angelman Syndrome

Published:2005-01-14 Issue: Volume: Page:
ISSN:
Container-title:Management of Genetic Syndromes
language:
Short-container-title:

Author:

Williams Charles A.

Publisher

John Wiley & Sons, Inc.

Reference44 articles.

1. Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints;Amos-Landgraf;Am J Hum Genet,1999

2. ��Puppet�� children: A report on three cases;Angelman;Dev Med Child Neurol,1965

3. Diagnostic testing for Prader-Willi and Angelman syndromes: Report of the ASHG/ACMG Test and Technology Transfer Committee;Am J Hum Genet,1996

4. Screening for UBE3A gene mutations in a group of Angelman syndrome patients selected according to non-stringent clinical criteria;Baumer;Hum Genet,1999

5. Angelman syndrome due to paternal uniparental disomy of chromosome 15: A milder phenotype? [see comments];Bottani;Am J Med Genet,1994

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Epilepsy in Angelman syndrome;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2022

2. Bibliography;The Psychology of Humor;2018

3. Chromosomal disorders associated with epilepsy;Epileptic Disorders;2005-09

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