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Clinical Genetics|August 22, 2014
Immunologic assessment and KMT2D mutation detection in Kabuki syndromeJ-L Lin, W-I Lee, J-L Huang, et al.
Pediatric Research|August 29, 2000
Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotypeB W Weston, J L Lin, J Muenzer, et al.
European Journal of Clinical Investigation|November 22, 2008
Renin-angiotensin system gene polymorphisms and diastolic heart failureC-K Wu, C-T Tsai, J-J Hwang, et al.
The American Journal of Cardiology|September 8, 2001
Dual-site atrial pacing for atrial fibrillation in patients without bradycardiaC P Lau, H F Tse, C M Yu, et al.
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