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A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function
Molecular Genetics & Genomic Medicine, 4 (2016), 5; 557-567. https://doi.org/10.1002/mgg3.234

Dreßen, Martina; Lahm, Harald; Lahm, Armin; Wolf, Klaudia; Doppler, Stefanie; Deutsch, Marcus-André; Cleuziou, Julie; Pabst von Ohain, Jelena; Schön, Patric; Ewert, Peter; Malčić, Ivan; Lange, Rüdiger; Krane, Markus

Citirajte ovaj rad

Dreßen, M., Lahm, H., Lahm, A., Wolf, K., Doppler, S., Deutsch, M. A. ... Krane, M. (2016). A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function. Molecular Genetics & Genomic Medicine, 4. (5), 557-567. doi: 10.1002/mgg3.234

Dreßen, Martina, et al. "A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function." Molecular Genetics & Genomic Medicine, vol. 4, br. 5, 2016, str. 557-567. https://doi.org/10.1002/mgg3.234

Dreßen, Martina, Harald Lahm, Armin Lahm, Klaudia Wolf, Stefanie Doppler, Marcus André Deutsch, Julie Cleuziou, et al. "A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function." Molecular Genetics & Genomic Medicine 4, br. 5 (2016): 557-567. https://doi.org/10.1002/mgg3.234

Dreßen, M., et al. (2016) 'A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function', Molecular Genetics & Genomic Medicine, 4(5), str. 557-567. doi: 10.1002/mgg3.234

Dreßen M, Lahm H, Lahm A, Wolf K, Doppler S, Deutsch MA, i sur.. A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function. Molecular Genetics & Genomic Medicine [Internet]. 14.07.2016. [pristupljeno 30.05.2024.];4(5):557-567. doi: 10.1002/mgg3.234

M. Dreßen, et al., "A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function", Molecular Genetics & Genomic Medicine, vol. 4, br. 5, str. 557-567, Srpanj 2016. [Online]. Dostupno na: https://urn.nsk.hr/urn:nbn:hr:105:788642. [Citirano: 30.05.2024.]

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