Clinical characterization of a Korean case with 3p25 deletion
Author:
Affiliation:
1. Department of Pediatrics, Asan Medical Center Children’s Hospital, University of Ulsan College of Medicine, Seoul, Korea
2. Medical Genetics Center, Asan Medical Center Children’s Hospital, University of Ulsan College of Medicine, Seoul, Korea
Publisher
Korean Society of Medical Genetics
Subject
General Medicine
Link
http://pdf.medrang.co.kr/JGM/2014/011/KSMGG6_2014_v11n1_36.pdf
Reference20 articles.
1. CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior
2. FISH and array-CGH analysis of a complex chromosome 3 aberration suggests that loss ofCNTN4 andCRBN contributes to mental retardation in 3pter deletions
3. Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.
4. Molecular characterization of a patient with 3p deletion syndrome and a review of the literature
5. A case of partial trisomy 3p syndrome with rare clinical manifestations
Cited by 2 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. The first Korean case of a newborn with 3p26 microdeletion and 5q35 microduplication inherited from paternal balanced translocation;Journal of Genetic Medicine;2021-06-30
2. Familiar del3p syndrome: The uncertainty of the prognosis. A case report;Clinical Case Reports;2021-03-09
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