Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies.

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Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis.Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic Changes.ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome.

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Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies.

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2013 nî lūn-bûn

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Chromosomal microaberrations i ...... ity, and congenital anomalies.

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Chromosomal microaberrations i ...... ity, and congenital anomalies.

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Chromosomal microaberrations i ...... ity, and congenital anomalies.

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Chromosomal microaberrations i ...... ity, and congenital anomalies.

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Chromosomal microaberrations i ...... ity, and congenital anomalies.

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Chromosomal microaberrations i ...... ity, and congenital anomalies.

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P2860

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.

Interpretation of array comparative genome hybridization data: a major challenge.

Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy.

Copy number variants in adult patients with Lennox-Gastaut syndrome features.

Genetically complex epilepsies, copy number variants and syndrome constellations.

Epilepsy in children.

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.

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Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies.

about

P2860

P2860

Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies.

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