A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation
Author:
Publisher
BMJ
Subject
Genetics(clinical),Genetics
Cited by 36 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. Restoration of functional PAX3 transcriptional factor enhanced neuronal differentiation in PAX3b isoform-depleted neuroblastoma cells;Cell and Tissue Research;2022-11-15
2. Fluoxetine Affects Differentiation of Midbrain Dopaminergic Neurons In Vitro;Molecular Pharmacology;2018-08-16
3. Genomic microarray technologies for the cytogenetics laboratory;The AGT Cytogenetics Laboratory Manual;2017-03-04
4. Deletion 2q37 syndrome: Cognitive-behavioral trajectories and autistic features related to breakpoint and deletion size;American Journal of Medical Genetics Part A;2016-06-09
5. Restricted Pax3 Deletion within the Neural Tube Results in Congenital Hydrocephalus;Journal of Developmental Biology;2016-02-01
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