41 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
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Active epilepsy in mentally retarded children. II. Etiology and reduced pre– and perinatal optimality
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