Electroclinical features of epilepsy in patients with InvDup(15)
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology,General Medicine
Reference35 articles.
1. Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome;Donlon;Proc Natl Acad Sci U S A,1986
2. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11–q13);Christian;Hum Mol Genet,1999
3. The invdup(15) or idic(15) syndrome: a clinically recognizable neurogenetic disorder;Battaglia;Brain Dev,2005
4. Mild generalized epilepsy and developmental disorder associated with large inv dup(15);Chifari;Epilepsia,2002
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1. Epilepsy, EEG and chromosomal rearrangements;Epilepsia Open;2024-06-04
2. Molecular genetic management of epilepsy;Clinical Molecular Medicine;2020
3. What is the role of next generation sequencing in status epilepticus?;Epilepsy & Behavior;2019-12
4. Behavioral characterization of dup15q syndrome: Toward meaningful endpoints for clinical trials;American Journal of Medical Genetics Part A;2019-10-26
5. Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of Patients;International Journal of Molecular Sciences;2019-10-05
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