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	1.	Detection of ubiquitous and heterogeneous mutations in cell-free DNA from patients with early-stage non-small-cell lung cancer. [electronic resource] by Jamal-Hanjani, M Wilson, G A Horswell, S Mitter, R Sakarya, O Constantin, T Salari, R Kirkizlar, E Sigurjonsson, S Pelham, R Kareht, S Zimmermann, B Swanton, C Producer: 20171221 In: Annals of oncology : official journal of the European Society for Medical Oncology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome. [electronic resource] by Gross, S J Stosic, M McDonald-McGinn, D M Bassett, A S Norvez, A Dhamankar, R Kobara, K Kirkizlar, E Zimmermann, B Wayham, N Babiarz, J E Ryan, A Jinnett, K N Demko, Z Benn, P Producer: 20161031 In: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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