Investigation ofTBR1Hemizygosity: Four Individuals with 2q24 Microdeletions-Reference-Cited by-同舟云学术

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Investigation ofTBR1Hemizygosity: Four Individuals with 2q24 Microdeletions

Published:2012 Issue:3 Volume:3 Page:102-112
ISSN:1661-8777
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Traylor R.N.,Dobyns W.B.,Rosenfeld J.A.,Wheeler P.,Spence J.E.,Bandholz A.M.,Bawle E.V.,Carmany E.P.,Powell C.M.,Hudson B.,Schultz R.A.,Shaffer L.G.,Ballif B.C.

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics

Cited by 31 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Transition from Animal-Based to Human Induced Pluripotent Stem Cells (iPSCs)-Based Models of Neurodevelopmental Disorders: Opportunities and Challenges;Cells;2023-02-07

2. A novel chromosome 2q24.3‐q32.1 microdeletion in a fetus with multiple malformations;Journal of Clinical Laboratory Analysis;2022-07-12

3. Tbr1 Misexpression Alters Neuronal Development in the Cerebral Cortex;Molecular Neurobiology;2022-07-04

4. Bilateral Coronal Synostosis and Mega Cisterna Magna: A Case Report;Cureus;2022-06-07

5. Dietary zinc supplementation rescues fear-based learning and synaptic function in the Tbr1+/− mouse model of autism spectrum disorders;Molecular Autism;2022-03-18

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