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New clinical molecular diagnostic methods for congenital and inherited heart disease

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Pages 9-24 | Published online: 08 Dec 2010

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Samira Kalayinia, Hamidreza Goodarzynejad, Majid Maleki & Nejat Mahdieh. (2018) Next generation sequencing applications for cardiovascular disease. Annals of Medicine 50:2, pages 91-109.
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Shafi Mahmud, Suvro Biswas, Shamima Afrose, Mohasana Akter Mita, Md. Robiul Hasan, Mst. Sharmin Sultana Shimu, Gobindo Kumar Paul, Sanghyun Chung, Md. Abu Saleh, Sultan Alshehri, Momammed M. Ghoneim, Maha Alruwaily & Bonglee Kim. (2022) Use of Next-Generation Sequencing for Identifying Mitochondrial Disorders. Current Issues in Molecular Biology 44:3, pages 1127-1148.
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Maria Kulecka, Andrzej Habior, Agnieszka Paziewska, Krzysztof Goryca, Michalina Dąbrowska, Filip Ambrozkiewicz, Bożena Walewska-Zielecka, Andrzej Gabriel, Michal Mikula & Jerzy Ostrowski. (2017) Clinical Applicability of Whole-Exome Sequencing Exemplified by a Study in Young Adults with the Advanced Cryptogenic Cholestatic Liver Diseases. Gastroenterology Research and Practice 2017, pages 1-8.
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J. P. Van Tintelen, P. G. Pieper, K. Y. Van Spaendonck-Zwarts & M. P. Van Den Berg. (2014) Pregnancy, cardiomyopathies, and genetics. Cardiovascular Research 101:4, pages 571-578.
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Birgit Sikkema-Raddatz, Lennart F. Johansson, Eddy N. de Boer, Rowida Almomani, Ludolf G. Boven, Maarten P. van den Berg, Karin Y. van Spaendonck-Zwarts, J. Peter van Tintelen, Rolf H. Sijmons, Jan D. H. Jongbloed & Richard J. Sinke. (2013) Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics. Human Mutation 34:7, pages 1035-1042.
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Gillian M BlueEdwin P KirkGary F ShollerRichard P HarveyDavid S Winlaw. (2012) Congenital heart disease: current knowledge about causes and inheritance. Medical Journal of Australia 197:3, pages 155-159.
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