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	1.	Exercise and β-blocker therapy recommendations for inherited arrhythmogenic conditions. [electronic resource] by Christian, Susan Somerville, Martin Taylor, Sherry Atallah, Joseph Producer: 20170208 In: Cardiology in the young vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Physical activity restriction for children and adolescents diagnosed with an inherited arrhythmia or cardiomyopathy and its impact on body mass index. [electronic resource] by Christian, Susan Somerville, Martin Giuffre, Michael Atallah, Joseph Producer: 20191111 In: Journal of cardiovascular electrophysiology vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	When to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy. [electronic resource] by Christian, Susan Somerville, Martin Taylor, Sherry Atallah, Joseph Producer: 20190926 In: Circulation. Genomic and precision medicine vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Homocysteine is not associated with global motor or cognitive measures in nondemented older Parkinson's disease patients. [electronic resource] by Camicioli, Richard M Bouchard, Thomas P Somerville, Martin J Producer: 20090608 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)
	5.	Defining the role of laboratory genetic counselor. [electronic resource] by Christian, Susan Lilley, Margaret Hume, Stacey Scott, Patrick Somerville, Martin Producer: 20121030 In: Journal of genetic counseling vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Integration of combined heteroduplex/restriction fragment length polymorphism analysis on an electrophoresis microchip for the detection of hereditary haemochromatosis. [electronic resource] by Footz, Tim Somerville, Martin J Tomaszewski, Robert Elyas, Basil Backhouse, Christopher J Producer: 20040416 In: The Analyst vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Heteroduplex-based genotyping with microchip electrophoresis and dHPLC. [electronic resource] by Footz, Tim Somerville, Martin J Tomaszewski, Robert Sprysak, Kathleen A Backhouse, Christopher J Producer: 20041021 In: Genetic testing vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	The impact of physical activity modification on the well-being of a cohort of children with an inherited arrhythmia or cardiomyopathy. [electronic resource] by Christian, Susan Somerville, Martin Taylor, Sherry Spence, John C Giuffre, Michael Atallah, Joseph Producer: 20210211 In: Cardiology in the young vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots. [electronic resource] by Whiteside, Darcy McLeod, Ross Graham, Gail Steckley, Jamie L Booth, Karen Somerville, Martin J Andrew, Susan E Producer: 20020215 In: Cancer research vol. 62 Availability: No items available. Save to lists Add to cart (remove)
	10.	Phenotype-genotype characterization of alpha-thalassemia mental retardation syndrome due to isolated monosomy of 16p13.3. [electronic resource] by Gibson, William T Harvard, Chansonette Qiao, Ying Somerville, Martin J Lewis, M E Suzanne Rajcan-Separovic, Evica Producer: 20080225 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cells. [electronic resource] by McDaniel, Lisa D Tomkins, Darrell J Stanbridge, Eric J Somerville, Martin J Friedberg, Errol C Schultz, Roger A Producer: 20050829 In: American journal of human genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Uptake of Predictive Genetic Testing and Cardiac Evaluation for Children at Risk for an Inherited Arrhythmia or Cardiomyopathy. [electronic resource] by Christian, Susan Atallah, Joseph Clegg, Robin Giuffre, Michael Huculak, Cathleen Dzwiniel, Tara Parboosingh, Jillian Taylor, Sherryl Somerville, Martin Producer: 20190304 In: Journal of genetic counseling vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Newborn screening for cystic fibrosis in Alberta: Two years of experience. [electronic resource] by Lilley, Margaret Christian, Susan Hume, Stacey Scott, Patrick Montgomery, Mark Semple, Lisa Zuberbuhler, Peter Tabak, Joan Bamforth, Fiona Somerville, Martin J Producer: 20111110 In: Paediatrics & child health vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Risk factors for development of dementia in a unique six-year cohort study. I. An exploratory, pilot study of involvement of the E4 allele of apolipoprotein E, mutations of the hemochromatosis-HFE gene, type 2 diabetes, and stroke. [electronic resource] by Percy, Maire Somerville, Martin J Hicks, Mark Garcia, Angeles Colelli, Teresa Wright, Emily Kitaygorodsky, Julia Jiang, Amy Ho, Valerie Parpia, Alyssa Wong, Michael K Producer: 20140817 In: Journal of Alzheimer's disease : JAD vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	GDF6, a novel locus for a spectrum of ocular developmental anomalies. [electronic resource] by Asai-Coakwell, Mika French, Curtis R Berry, Karyn M Ye, Ming Koss, Ron Somerville, Martin Mueller, Rosemary van Heyningen, Veronica Waskiewicz, Andrew J Lehmann, Ordan J Producer: 20070313 In: American journal of human genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Discrepant HIV results resolved by human DNA testing. [electronic resource] by Tang, Julian W Adachi, Dena Gunning, Hans Marian-Dyer, Carol Hume, Stacey Taylor, Sherryl Haase, Shelagh Vicen, Leanne Benedet, Marlin Chow, Anthony Somerville, Martin Hicks, Mark Tipples, Graham Producer: 20150520 In: Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Toward optimal detection of the common prenatal aneuploidies by quantitative fluorescent-polymerase chain reaction: comparison of two commercial assays. [electronic resource] by Scott, Patrick Podemski, Lynn Baptista Wyatt, Kelly Walker, Christine Haase, Shelagh M Elyas, Basil G Sprysak, Kathleen A Lilley, Margaret Christian, Susan Hicks, Mark Somerville, Martin J Hume, Stacey L Producer: 20130114 In: Genetic testing and molecular biomarkers vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease. [electronic resource] by Christiansen, Jesse Dyck, John D Elyas, Basil G Lilley, Margaret Bamforth, J Stephen Hicks, Mark Sprysak, Kathleen A Tomaszewski, Robert Haase, Shelagh M Vicen-Wyhony, Leanne M Somerville, Martin J Producer: 20041217 In: Circulation research vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Severe expressive-language delay related to duplication of the Williams-Beuren locus. [electronic resource] by Somerville, Martin J Mervis, Carolyn B Young, Edwin J Seo, Eul-Ju del Campo, Miguel Bamforth, Stephen Peregrine, Ella Loo, Wayne Lilley, Margaret Pérez-Jurado, Luis A Morris, Colleen A Scherer, Stephen W Osborne, Lucy R Producer: 20051028 In: The New England journal of medicine vol. 353 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Microduplication and triplication of 22q11.2: a highly variable syndrome. [electronic resource] by Yobb, Twila M Somerville, Martin J Willatt, Lionel Firth, Helen V Harrison, Karen MacKenzie, Jennifer Gallo, Natasha Morrow, Bernice E Shaffer, Lisa G Babcock, Melanie Chernos, Judy Bernier, Francois Sprysak, Kathy Christiansen, Jesse Haase, Shelagh Elyas, Basil Lilley, Margaret Bamforth, Steven McDermid, Heather E Producer: 20050616 In: American journal of human genetics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 23 results.