The utility of molecular diagnostics in tumour surveillance in Beckwith-Wiedemann syndrome – clinical genetics point of view in light of a case report
Pediatria Polska(2018)
Abstract
ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Drankowska J, Kos M, Kościuk A, Nurzyńska-Flak J. The utility of molecular diagnostics in tumour surveillance in Beckwith-Wiedemann syndrome – clinical genetics point of view in light of a case report. Pediatria Polska - Polish Journal of Paediatrics. 2018;93(6):479-483. doi:10.5114/polp.2018.82657. APA Drankowska, J., Kos, M., Kościuk, A., & Nurzyńska-Flak, J. (2018). The utility of molecular diagnostics in tumour surveillance in Beckwith-Wiedemann syndrome – clinical genetics point of view in light of a case report. Pediatria Polska - Polish Journal of Paediatrics, 93(6), 479-483. https://doi.org/10.5114/polp.2018.82657 Chicago Drankowska, Justyna, Michał Kos, Andrzej Kościuk, and Joanna Nurzyńska-Flak. 2018. "The utility of molecular diagnostics in tumour surveillance in Beckwith-Wiedemann syndrome – clinical genetics point of view in light of a case report". Pediatria Polska - Polish Journal of Paediatrics 93 (6): 479-483. doi:10.5114/polp.2018.82657. Harvard Drankowska, J., Kos, M., Kościuk, A., and Nurzyńska-Flak, J. (2018). The utility of molecular diagnostics in tumour surveillance in Beckwith-Wiedemann syndrome – clinical genetics point of view in light of a case report. Pediatria Polska - Polish Journal of Paediatrics, 93(6), pp.479-483. https://doi.org/10.5114/polp.2018.82657 MLA Drankowska, Justyna et al. "The utility of molecular diagnostics in tumour surveillance in Beckwith-Wiedemann syndrome – clinical genetics point of view in light of a case report." Pediatria Polska - Polish Journal of Paediatrics, vol. 93, no. 6, 2018, pp. 479-483. doi:10.5114/polp.2018.82657. Vancouver Drankowska J, Kos M, Kościuk A, Nurzyńska-Flak J. The utility of molecular diagnostics in tumour surveillance in Beckwith-Wiedemann syndrome – clinical genetics point of view in light of a case report. Pediatria Polska - Polish Journal of Paediatrics. 2018;93(6):479-483. doi:10.5114/polp.2018.82657.
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Key words
clinical genetics point,syndrome,molecular diagnostics,beckwith-wiedemann
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