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Genetics
Citations 1-10 of 132 total displayed.
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Most recent content
(15 Sep 2009):
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- Analysis
Genetic diagnosis of embryos: Clear explanation, not rhetoric, is needed
- Chantal Bouffard, Stéphane Viville, and Bartha Maria Knoppers
Can. Med. Assoc. J. 2009; 181: 387-391.
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Past content
(since Jul 1999):
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- News
Prenatal DNA test raises both hopes and worries
- Roger Collier
Can. Med. Assoc. J. 2009; 180: 705-706.
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- News
United States government grows a family health tree, helping people trace hand-me-down genetic risks
- Cal Woodward
Can. Med. Assoc. J. 2009; 180: 707.
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- News
For the record
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Can. Med. Assoc. J. 2009; 180: 283.
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- Practice
A patient with loss of vision in the right eye and neurofibromatosis type 1
- Nicola Mumoli, MD, Marco Cei, MD, Carlo Bartolomei, MD, and Vania Pirillo, MD
Can. Med. Assoc. J. 2009; 180: 203-206.
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- Commentary
Unravelling the contributions of social, environmental and genetic factors to health differences
- Vence L. Bonham, JD and Erin M. Ramos, PhD MPH
Can. Med. Assoc. J. 2008; 179: 629-630.
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- Research
A population-based analysis of the health experience of African Nova Scotians
- Steve Kisely, MD MSc, Mikiko Terashima, MSc, and Don Langille, MD MHSc
Can. Med. Assoc. J. 2008; 179: 653-658.
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- Practice
Diagnosis and treatment of dementia: 1. Risk assessment and primary prevention of Alzheimer disease
- Christopher Patterson, MD, John W. Feightner, MD MSc, Angeles Garcia, MD PhD, G.-Y. Robin Hsiung, MD MHSc, Christopher MacKnight, MD MSc, and A. Dessa Sadovnick, PhD
Can. Med. Assoc. J. 2008; 178: 548-556.
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- Commentary
Should physicians warn patients' relatives of genetic risks?
- Mireille Lacroix, LLM, Gillian Nycum, BCL LLB, Béatrice Godard, PhD, and Bartha Maria Knoppers, PhD
Can. Med. Assoc. J. 2008; 178: 593-595.
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- Practice
Recognizing a common genetic syndrome: 22q11.2 deletion syndrome
- Ronak K. Kapadia, BSc and Anne S. Bassett, MD
Can. Med. Assoc. J. 2008; 178: 391-393.
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