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	1.	Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome? [electronic resource] by Yu, Andrea C Zambrano, Regina M Cristian, Ingrid Price, Sue Bernhard, Birgitta Zucker, Marc Venkateswaran, Sunita McGowan-Jordan, Jean Armour, Christine M Producer: 20171201 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Evaluation of the quality of clinical data collection for a pan-Canadian cohort of children affected by inherited metabolic diseases: lessons learned from the Canadian Inherited Metabolic Diseases Research Network. [electronic resource] by Tingley, Kylie Lamoureux, Monica Pugliese, Michael Geraghty, Michael T Kronick, Jonathan B Potter, Beth K Coyle, Doug Wilson, Kumanan Kowalski, Michael Austin, Valerie Brunel-Guitton, Catherine Buhas, Daniela Chan, Alicia K J Dyack, Sarah Feigenbaum, Annette Giezen, Alette Goobie, Sharan Greenberg, Cheryl R Ghai, Shailly Jain Inbar-Feigenberg, Michal Karp, Natalya Kozenko, Mariya Langley, Erica Lines, Matthew Little, Julian MacKenzie, Jennifer Maranda, Bruno Mercimek-Andrews, Saadet Mohan, Connie Mhanni, Aizeddin Mitchell, Grant Mitchell, John J Nagy, Laura Napier, Melanie Pender, Amy Potter, Murray Prasad, Chitra Ratko, Suzanne Salvarinova, Ramona Schulze, Andreas Siriwardena, Komudi Sondheimer, Neal Sparkes, Rebecca Stockler-Ipsiroglu, Sylvia Trakadis, Yannis Turner, Lesley Van Karnebeek, Clara Vallance, Hilary Vandersteen, Anthony Walia, Jagdeep Wilson, Ashley Wilson, Brenda J Yu, Andrea C Yuskiv, Nataliya Chakraborty, Pranesh Producer: 20210618 In: Orphanet journal of rare diseases vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)