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	1.	Juvenile hemochromatosis due to homozygosity for the G320V mutation in the HJV gene with fatal outcome. [electronic resource] by Brakensiek, Kai Fegbeutel, Christine Mälzer, Madeleine Strüber, Martin Kreipe, Hans Stuhrmann, Manfred Producer: 20100225 In: Clinical genetics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	NCAM2 deletion in a boy with macrocephaly and autism: Cause, association or predisposition? [electronic resource] by Scholz, Caroline Steinemann, Doris Mälzer, Madeleine Roy, Mandy Arslan-Kirchner, Mine Illig, Thomas Schmidtke, Jörg Stuhrmann, Manfred Producer: 20170207 In: European journal of medical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome. [electronic resource] by Wessels, Kathrin Bohnhorst, Bettina Luhmer, Ingrid Morlot, Susanne Bohring, Axel Jonasson, Jon Epplen, Jörg T Gadzicki, Dorothea Glaser, Stefanie Göhring, Gudrun Mälzer, Madeleine Hein, Anke Arslan-Kirchner, Mine Stuhrmann, Manfred Schmidtke, Jörg Pabst, Brigitte Producer: 20110111 In: European journal of medical genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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