Molecular Syndromology,volume 7,issue 4  (08-2016)

Period of time： 2016年4期

Publisher： Karger

Founded in： 2010

Total resources： 43

E-ISSN： 1661-8777|7|4

ISSN： 1661-8769

Subject： Q3 Genetics

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Molecular Syndromology,volume 7,issue 4

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Molecular Syndromology,volume 7,issue 4 , Vol. 7, Iss. 4, 2016-09 , pp. 165-168

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Towards a Molecular Syndromology of the Epilepsies

Molecular Syndromology,volume 7,issue 4 , Vol. 7, Iss. 4, 2016-08 , pp. 169-171

Karger

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Understanding Genotypes and Phenotypes in Epileptic Encephalopathies

Molecular Syndromology,volume 7,issue 4 , Vol. 7, Iss. 4, 2016-08 , pp. 172-181

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Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in SCN2A

Molecular Syndromology,volume 7,issue 4 , Vol. 7, Iss. 4, 2016-07 , pp. 182-188

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Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures

Molecular Syndromology,volume 7,issue 4 , Vol. 7, Iss. 4, 2016-07 , pp. 189-196

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Seizures and Epilepsies due to Channelopathies and Neurotransmitter Receptor Dysfunction: A Parallel between Genetic and Immune Aspects

Molecular Syndromology,volume 7,issue 4 , Vol. 7, Iss. 4, 2016-07 , pp. 197-209

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Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies

Molecular Syndromology,volume 7,issue 4 , Vol. 7, Iss. 4, 2016-08 , pp. 210-219

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Genetic Basis of Brain Malformations

Molecular Syndromology,volume 7,issue 4 , Vol. 7, Iss. 4, 2016-08 , pp. 220-233

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Exome Sequencing Fails to Identify the Genetic Cause of Aicardi Syndrome

Molecular Syndromology,volume 7,issue 4 , Vol. 7, Iss. 4, 2016-08 , pp. 234-238

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Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome

Molecular Syndromology,volume 7,issue 4 , Vol. 7, Iss. 4, 2016-08 , pp. 239-246

Karger

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