Isolated 9p Duplication With der(Y)t(Y;9)(q12;p13.2) in a Male Patient With Cardiac Defect and Mental Retardation Confirmed by Chromosomal Microarray
Author:
Affiliation:
1. Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea
2. Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Korea
Funder
National Research Foundation of Korea
Ministry of Education, Science and Technology
Publisher
Annals of Laboratory Medicine
Subject
Biochemistry (medical),Clinical Biochemistry,General Medicine
Link
http://synapse.koreamed.org/pdf/10.3343/alm.2016.36.2.191
Reference10 articles.
1. Duplication 9p and their implication to phenotype
2. Maternal origin of a unique extra chromosome, der(9)(pter?q13::q13?q12:) in a girl with typical trisomy 9p syndrome
3. Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).
4. Clinical and molecular delineation of duplication 9p24.3q21.11 in a patient with psychotic behavior
5. A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation
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. 9p triszómia és a klinikai sokszínűség: egy váratlan megjelenésű eset ismertetése;Orvosi Hetilap;2018-11
2. Mosaic Tetrasomy of 9p24.3q21.11 postnatally identified in an infant born with multiple congenital malformations: a case report;BMC Pediatrics;2018-09-07
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