42 research outputs found
Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes
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Angelman Syndrome in Three Siblings: Genetic Model of Epilepsy Associated with Chromosomal DNA Deletion of the GABA A
No full textAngelman Syndrome in Three Siblings: Characteristic Epileptic Seizures and EEG Abnormalities
No full textDiagnosis of the Prader-Willi syndrome by proving the absence of the unmethylated PW71 DNA fragment
No full textAngelman syndrome: Consensus for diagnostic criteria
Full text linkThe Scientific and Research Advisory Committee of the Angelman Syndrome Foundation recently solicited input from scientists involved in the study of Angelman syndrome to establish consensus about the clinical pro- file and diagnostic criteria of Angelman syndrome
