Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome-Reference-Cited by-同舟云学术

Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome

Published:2020-01-31 Issue: Volume:11 Page:
ISSN:1664-2295
Container-title:Frontiers in Neurology
language:
Short-container-title:Front. Neurol.

Author:

Welby Lauren,Caudill Hailey,Yitsege Gelila,Hamad Ali,Bunyak Filiz,Zohn Irene E.,Maynard Thomas,LaMantia Anthony-Samuel,Mendelowitz David,Lever Teresa E.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Frontiers Media SA

Subject

Clinical Neurology,Neurology

Reference47 articles.

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3. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study;Ryan;J Med Genet.,1997

4. Cognitive ability is associated with altered medial frontal cortical circuits in the LgDel mouse model of 22q11.2DS;Meechan;Cereb Cortex.,2015

5. 22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development;Maynard;Hum Mol Genet.,2013

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