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	1.	Clinical study of two brothers with a novel 33 bp duplication in the ARX gene. [electronic resource] by Demos, Michelle K Fullston, Tod Partington, Michael W Gécz, Jozef Gibson, William T Producer: 20090923 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction. [electronic resource] by Demos, Michelle K Macri, Vincenzo Farrell, Kevin Nelson, Tanya N Chapman, Kristine Accili, Eric Armstrong, Linlea Producer: 20090728 In: Movement disorders : official journal of the Movement Disorder Society vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	6-pyruvoyl-tetrahydropterin synthase deficiency with mild hyperphenylalaninemia. [electronic resource] by Demos, Michelle K Waters, Paula J Vallance, Hilary D Lillquist, Yolanda Makhseed, Nawal Hyland, Keith Blau, Nenad Connolly, Mary B Producer: 20050906 In: Annals of neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions. [electronic resource] by Adam, Shelin Birch, Patricia H Coe, Rachel R Bansback, Nick Jones, Adrian L Connolly, Mary B Demos, Michelle K Toyota, Eric B Farrer, Matthew J Friedman, Jan M Publication details: Journal of genetic counseling Jul 2018 In: Journal of genetic counseling Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A novel recurrent mutation in ATP1A3 causes CAPOS syndrome. [electronic resource] by Demos, Michelle K van Karnebeek, Clara Dm Ross, Colin Jd Adam, Shelin Shen, Yaoqing Zhan, Shing Hei Shyr, Casper Horvath, Gabriella Suri, Mohnish Fryer, Alan Jones, Steven Jm Friedman, Jan M Producer: 20141112 In: Orphanet journal of rare diseases vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Characterization of a new X-linked mental retardation syndrome with microcephaly, cortical malformation, and thin habitus. [electronic resource] by du Souich, Christèle Chou, Athena Yin, Jingyi Oh, Tracey Nelson, Tanya N Hurlburt, Jane Arbour, Laura Friedlander, Robin McGillivray, Barbara C Tyshchenko, Nataliya Rump, Andreas Poskitt, Kenneth J Demos, Michelle K Van Allen, Margot I Boerkoel, Cornelius F Producer: 20100106 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders. [electronic resource] by Faundes, Víctor Newman, William G Bernardini, Laura Canham, Natalie Clayton-Smith, Jill Dallapiccola, Bruno Davies, Sally J Demos, Michelle K Goldman, Amy Gill, Harinder Horton, Rachel Kerr, Bronwyn Kumar, Dhavendra Lehman, Anna McKee, Shane Morton, Jenny Parker, Michael J Rankin, Julia Robertson, Lisa Temple, I Karen Banka, Siddharth Producer: 20181211 In: American journal of human genetics vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)