Your search returned 19 results.

Results
	1.	Genetics and Precision Medicine: Heritable Thoracic Aortic Disease. [electronic resource] by Demo, Erin Rigelsky, Christina Rideout, Andrea L Graf, Madeline Pariani, Mitchel Regalado, Ellen MacCarrick, Gretchen Producer: 20191008 In: The Medical clinics of North America vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A family with Classical Ehlers-Danlos Syndrome (cEDS), mild bone fragility and without vascular complications, caused by the p.Arg312Cys mutation in COL1A1. [electronic resource] by Duong, June Rideout, Andrea MacKay, Sara Beis, Jill Parkash, Sandhya Schwarze, Ulrike Horne, S Gabrielle Vandersteen, Anthony Producer: 20201019 In: European journal of medical genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel ADAMTS17 variant that causes Weill-Marchesani syndrome 4 alters fibrillin-1 and collagen type I deposition in the extracellular matrix. [electronic resource] by Karoulias, Stylianos Z Beyens, Aude Balic, Zerina Symoens, Sofie Vandersteen, Anthony Rideout, Andrea L Dickinson, John Callewaert, Bert Hubmacher, Dirk Producer: 20210526 In: Matrix biology : journal of the International Society for Matrix Biology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Interactive genetic counseling role-play: a novel educational strategy for family physicians. [electronic resource] by Blaine, Sean M Carroll, June C Rideout, Andrea L Glendon, Gord Meschino, Wendy Shuman, Cheryl Telner, Deanna Van Iderstine, Natasha Permaul, Joanne Producer: 20080617 In: Journal of genetic counseling vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genetics: schizophrenia. [electronic resource] by Rideout, Andrea L Carroll, June C Blaine, Sean M Cremin, Carol Dorman, Heather Gibbons, Clare A Honeywell, Christina Meschino, Wendy S Permaul, Joanne Allanson, Judith Producer: 20100311 In: Canadian family physician Medecin de famille canadien vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	6.	Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2. [electronic resource] by Guernsey, Duane L Jiang, Haiyan Evans, Susan C Ferguson, Meghan Matsuoka, Makoto Nightingale, Mathew Rideout, Andrea L Provost, Sylvie Bedard, Karen Orr, Andrew Dubé, Marie-Pierre Ludman, Mark Samuels, Mark E Producer: 20090715 In: American journal of human genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Maternal age-based prenatal screening for chromosomal disorders: attitudes of women and health care providers toward changes. [electronic resource] by Carroll, June C Rideout, Andrea Wilson, Brenda J Allanson, Judith Blaine, Sean Esplen, Mary Jane Farrell, Sandra Graham, Gail E MacKenzie, Jennifer Meschino, Wendy S Prakash, Preeti Shuman, Cheryl Taylor, Sherry Tobin, Stasey Producer: 20130712 In: Canadian family physician Medecin de famille canadien vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	8.	Mutation in the gene encoding ubiquitin ligase LRSAM1 in patients with Charcot-Marie-Tooth disease. [electronic resource] by Guernsey, Duane L Jiang, Haiyan Bedard, Karen Evans, Susan C Ferguson, Meghan Matsuoka, Makoto Macgillivray, Christine Nightingale, Mathew Perry, Scott Rideout, Andrea L Orr, Andrew Ludman, Mark Skidmore, David L Benstead, Timothy Samuels, Mark E Producer: 20101228 In: PLoS genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Phenotypic and molecular characterization of 19q12q13.1 deletions: a report of five patients. [electronic resource] by Chowdhury, Shimul Bandholz, Anne M Parkash, Sandhya Dyack, Sarah Rideout, Andrea L Leppig, Kathleen A Thiese, Heidi Wheeler, Patricia G Tsang, Marilyn Ballif, Blake C Shaffer, Lisa G Torchia, Beth S Ellison, Jay W Rosenfeld, Jill A Producer: 20150413 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Genetic education for primary care providers: improving attitudes, knowledge, and confidence. [electronic resource] by Carroll, June C Rideout, Andrea L Wilson, Brenda J Allanson, Judith Md Blaine, Sean M Esplen, Mary Jane Farrell, Sandra A Graham, Gail E MacKenzie, Jennifer Meschino, Wendy Miller, Fiona Prakash, Preeti Shuman, Cheryl Summers, Anne Taylor, Sherry Producer: 20100311 In: Canadian family physician Medecin de famille canadien vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	11.	None [electronic resource] by Hostetler, Ellen M Regalado, Ellen S Guo, Dong-Chuan Hanna, Nadine Arnaud, Pauline Muiño-Mosquera, Laura Callewaert, Bert Louis Lee, Kwanghyuk Leal, Suzanne M Wallace, Stephanie E Rideout, Andrea L Dyack, Sarah Aatre, Rajani D Boileau, Catherine De Backer, Julie Jondeau, Guillaume Milewicz, Dianna M Producer: 20200522 In: Journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man. [electronic resource] by Tuschl, Karin Clayton, Peter T Gospe, Sidney M Gulab, Shamshad Ibrahim, Shahnaz Singhi, Pratibha Aulakh, Roosy Ribeiro, Reinaldo T Barsottini, Orlando G Zaki, Maha S Del Rosario, Maria Luz Dyack, Sarah Price, Victoria Rideout, Andrea Gordon, Kevin Wevers, Ron A Chong, W K ''Kling'' Mills, Philippa B Publication details: American journal of human genetics 08 2016 In: American journal of human genetics vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man. [electronic resource] by Tuschl, Karin Clayton, Peter T Gospe, Sidney M Gulab, Shamshad Ibrahim, Shahnaz Singhi, Pratibha Aulakh, Roosy Ribeiro, Reinaldo T Barsottini, Orlando G Zaki, Maha S Del Rosario, Maria Luz Dyack, Sarah Price, Victoria Rideout, Andrea Gordon, Kevin Wevers, Ron A Chong, W K Kling Mills, Philippa B Producer: 20120713 In: American journal of human genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia. [electronic resource] by Guernsey, Duane L Jiang, Haiyan Campagna, Dean R Evans, Susan C Ferguson, Meghan Kellogg, Mark D Lachance, Mathieu Matsuoka, Makoto Nightingale, Mathew Rideout, Andrea Saint-Amant, Louis Schmidt, Paul J Orr, Andrew Bottomley, Sylvia S Fleming, Mark D Ludman, Mark Dyack, Sarah Fernandez, Conrad V Samuels, Mark E Producer: 20101104 In: Nature genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome. [electronic resource] by Guernsey, Duane L Matsuoka, Makoto Jiang, Haiyan Evans, Susan Macgillivray, Christine Nightingale, Mathew Perry, Scott Ferguson, Meghan LeBlanc, Marissa Paquette, Jean Patry, Lysanne Rideout, Andrea L Thomas, Aidan Orr, Andrew McMaster, Chris R Michaud, Jacques L Deal, Cheri Langlois, Sylvie Superneau, Duane W Parkash, Sandhya Ludman, Mark Skidmore, David L Samuels, Mark E Producer: 20110509 In: Nature genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4. [electronic resource] by Guernsey, Duane L Jiang, Haiyan Hussin, Julie Arnold, Marc Bouyakdan, Khalil Perry, Scott Babineau-Sturk, Tina Beis, Jill Dumas, Nadine Evans, Susan C Ferguson, Meghan Matsuoka, Makoto Macgillivray, Christine Nightingale, Mathew Patry, Lysanne Rideout, Andrea L Thomas, Aidan Orr, Andrew Hoffmann, Ingrid Michaud, Jacques L Awadalla, Philip Meek, David C Ludman, Mark Samuels, Mark E Producer: 20100728 In: American journal of human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Germline mutations in MAP3K6 are associated with familial gastric cancer. [electronic resource] by Gaston, Daniel Hansford, Samantha Oliveira, Carla Nightingale, Mathew Pinheiro, Hugo Macgillivray, Christine Kaurah, Pardeep Rideout, Andrea L Steele, Patricia Soares, Gabriela Huang, Weei-Yuarn Whitehouse, Scott Blowers, Sarah LeBlanc, Marissa A Jiang, Haiyan Greer, Wenda Samuels, Mark E Orr, Andrew Fernandez, Conrad V Majewski, Jacek Ludman, Mark Dyack, Sarah Penney, Lynette S McMaster, Christopher R Huntsman, David Bedard, Karen Producer: 20150702 In: PLoS genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium. [electronic resource] by Aronson, Melyssa Gallinger, Steven Cohen, Zane Cohen, Shlomi Dvir, Rina Elhasid, Ronit Baris, Hagit N Kariv, Revital Druker, Harriet Chan, Helen Ling, Simon C Kortan, Paul Holter, Spring Semotiuk, Kara Malkin, David Farah, Roula Sayad, Alain Heald, Brandie Kalady, Matthew F Penney, Lynette S Rideout, Andrea L Rashid, Mohsin Hasadsri, Linda Pichurin, Pavel Riegert-Johnson, Douglas Campbell, Brittany Bakry, Doua Al-Rimawi, Hala Alharbi, Qasim Kholaif Alharbi, Musa Shamvil, Ashraf Tabori, Uri Durno, Carol Producer: 20160627 In: The American journal of gastroenterology vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3. [electronic resource] by Schepers, Dorien Tortora, Giada Morisaki, Hiroko MacCarrick, Gretchen Lindsay, Mark Liang, David Mehta, Sarju G Hague, Jennifer Verhagen, Judith van de Laar, Ingrid Wessels, Marja Detisch, Yvonne van Haelst, Mieke Baas, Annette Lichtenbelt, Klaske Braun, Kees van der Linde, Denise Roos-Hesselink, Jolien McGillivray, George Meester, Josephina Maystadt, Isabelle Coucke, Paul El-Khoury, Elie Parkash, Sandhya Diness, Birgitte Risom, Lotte Scurr, Ingrid Hilhorst-Hofstee, Yvonne Morisaki, Takayuki Richer, Julie Désir, Julie Kempers, Marlies Rideout, Andrea L Horne, Gabrielle Bennett, Chris Rahikkala, Elisa Vandeweyer, Geert Alaerts, Maaike Verstraeten, Aline Dietz, Hal Van Laer, Lut Loeys, Bart Producer: 20190513 In: Human mutation vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)