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	1.	Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening. [electronic resource] by Handt, Maximilian Epplen, Andrea Hoffjan, Sabine Mese, Kemal Epplen, Jörg T Dekomien, Gabriele Producer: 20150724 In: Molecular and cellular probes vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	NDUFA2 complex I mutation leads to Leigh disease. [electronic resource] by Hoefs, Saskia J G Dieteren, Cindy E J Distelmaier, Felix Janssen, Rolf J R J Epplen, Andrea Swarts, Herman G P Forkink, Marleen Rodenburg, Richard J Nijtmans, Leo G Willems, Peter H Smeitink, Jan A M van den Heuvel, Lambert P Producer: 20080627 In: American journal of human genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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