Refining critical regions in 15q24 microdeletion syndrome pertaining to autism-Reference-Cited by-全球学者库

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Refining critical regions in 15q24 microdeletion syndrome pertaining to autism

Published:2020-01-18 Issue:4 Volume:183 Page:217-226
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Liu Yi¹^ORCID,Zhang Yanqing²,Zarrei Mehdi³,Dong Rui¹,Yang Xiaomeng¹,Zhao Dongmei²,Scherer Stephen W.³⁴^ORCID,Gai Zhongtao¹

Affiliation:

1. Pediatric Research Institute, Qilu Children's Hospital of Shandong University Ji'nan China

2. Pediatric Health Care Institute, Qilu Children's Hospital of Shandong University Ji'nan 250022 China

3. The Centre for Applied GenomicsThe Hospital for Sick Children Toronto Ontario Canada

4. McLaughlin Centre and Department of Molecular GeneticsUniversity of Toronto Toronto Ontario Canada

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.32778

Reference71 articles.

1. Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopment

2. A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report

3. BBS4 directly affects proliferation and differentiation of adipocytes

4. Genotypeâphenotype correlation in four 15q24 deleted patients identified by array-CGH

5. Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Cited by 3 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. Molecular Genetic Analysis of Newborns with Congenital Microcephaly;Neonatology;2022

2. Molecular and phenotypic characteristics of 15q24 microdeletion in pediatric patients with developmental disorders;Molecular Cytogenetics;2021-12

3. Neuroplastin in Neuropsychiatric Diseases;Genes;2021-09-26

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