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Dec 26, 2017 (publication date) through Jan 13, 2026
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World Journal of Cardiology
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1949-8462
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| Karunanithi Z, Vestergaard EM, Lauridsen MH. Transposition of the great arteries - a phenotype associated with 16p11.2 duplications? World J Cardiol 2017; 9(12): 848-852 [PMID: 29317992 DOI: 10.4330/wjc.v9.i12.848] |
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| ©2004-2026 Baishideng Publishing Group Inc. All rights reserved. 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA | |
| For: | Karunanithi Z, Vestergaard EM, Lauridsen MH. Transposition of the great arteries - a phenotype associated with 16p11.2 duplications? World J Cardiol 2017; 9(12): 848-852 [PMID: 29317992 DOI: 10.4330/wjc.v9.i12.848] |
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| URL: | https://www.wjgnet.com/1949-8462/full/v9/i12/848.htm |
| Number | Citing Articles |
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Chiara Auwerx, Zoltán Kutalik, Alexandre Reymond. The pleiotropic spectrum of proximal 16p11.2 CNVs. The American Journal of Human Genetics 2024; 111(11): 2309 doi: 10.1016/j.ajhg.2024.08.015
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| 2 |
Alessandra Suuberg. Phenotypic and Evolutionary Consequences of Deletion, Duplication, and Triplication at 16p11.2. SSRN Electronic Journal 2018; doi: 10.2139/ssrn.3185741
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| 3 |
Pilar Carrasco Salas, Reyes Granell Escobar, Ana Serrano Mira, Angustias Pérez Saldaña, Marta Cosculluela Vidal, Carlos Garrido, Ignacio Vázquez Rico. Findings in Chromosomal Microarray Analysis during Prenatal Diagnosis in High-Risk Individuals. Molecular Syndromology 2024; 16(5): 401 doi: 10.1159/000543064
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Rafaella Mergener, Lívia Polisseni Cotta Nascimento, Ana Kalise Böttcher, Marcela Rodrigues Nunes, Paulo Ricardo Gazzola Zen. What Can Really Be Considered a Syndrome? An Insight Based on 16p11.2 Microduplication. Cell Biochemistry and Function 2024; 42(7) doi: 10.1002/cbf.4121
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Majed J. Dasouki, Salma M. Wakil, Olfat Al-Harazi, Maarab Alkorashy, Nzioka P. Muiya, Editha Andres, Samya Hagos, Haya Aldusery, Nduna Dzimiri, Dilek Colak. New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia. OMICS: A Journal of Integrative Biology 2020; 24(1): 16 doi: 10.1089/omi.2019.0165
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Laurent Ehrlich, Siddharth K Prakash. Copy-number variation in congenital heart disease. Current Opinion in Genetics & Development 2022; 77: 101986 doi: 10.1016/j.gde.2022.101986
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Mikhail Vysotskiy, Xue Zhong, Tyne W. Miller-Fleming, Dan Zhou, Nancy J. Cox, Lauren A. Weiss. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. Genome Medicine 2021; 13(1) doi: 10.1186/s13073-021-00972-1
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