Focal Cortical Anomalies and Language Impairment in 16p11.2 Deletion and Duplication Syndrome.

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Syndromic autism spectrum disorders: moving from a clinically defined to a molecularly defined approach.Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis.

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Focal Cortical Anomalies and Language Impairment in 16p11.2 Deletion and Duplication Syndrome.

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2017年学术文章

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Focal Cortical Anomalies and L ...... tion and Duplication Syndrome.

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Focal Cortical Anomalies and L ...... tion and Duplication Syndrome.

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Focal Cortical Anomalies and L ...... tion and Duplication Syndrome.

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Focal Cortical Anomalies and L ...... tion and Duplication Syndrome.

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Focal Cortical Anomalies and L ...... tion and Duplication Syndrome.

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Focal Cortical Anomalies and L ...... tion and Duplication Syndrome.

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Benjamin Fuchs

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Emma Ben-Avi

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Karen Blackmon

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Orrin Devinsky

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Ruben Kuzniecky

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Sophie Green

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Thomas Thesen

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Xiuyuan Wang

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Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.

Cortical Surface-Based Analysis

Association between microdeletion and microduplication at 16p11.2 and autism

Detection of epileptogenic cortical malformations with surface-based MRI morphometry

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest

Measuring the thickness of the human cerebral cortex from magnetic resonance images

The arcuate fasciculus and the disconnection theme in language and aphasia: history and current state

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts.

A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.

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1-9

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scholarly article

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10.1093/CERCOR/BHX143

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2017-06-07T00:00:00Z

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28591836

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Focal Cortical Anomalies and Language Impairment in 16p11.2 Deletion and Duplication Syndrome.

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Focal Cortical Anomalies and Language Impairment in 16p11.2 Deletion and Duplication Syndrome.

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