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Journal of the American College of Cardiology|March 17, 2018
Cardiac Genetic Predisposition in Sudden Infant Death SyndromeDavid J Tester, Leonie C H Wong, Pritha Chanana, et al.
BMC Cardiovascular Disorders|July 25, 2019
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsyHariharan Raju, James S Ware, Jonathan R Skinner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 30, 2019
The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiencyNandaki Keshavan, Jose Abdenur, Glenn Anderson, et al.
Archives of Pathology & Laboratory Medicine|May 26, 2016
Sampling and Definitions of Placental Lesions: Amsterdam Placental Workshop Group Consensus StatementT Yee Khong, Eoghan E Mooney, Ilana Ariel, et al.
Lancet (London, England)|April 2, 2018
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control studyRoope Männikkö, Leonie Wong, David J Tester, et al.
Journal of the American College of Cardiology|April 29, 2017
Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death SyndromeNajim Lahrouchi, Hariharan Raju, Elisabeth M Lodder, et al.
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