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Heart Rhythm|April 2, 2020
Genetic testing in Polynesian long QT syndrome probands reveals a lower diagnostic yield and an increased prevalence of rare variantsAnnika Winbo, Nikki Earle, Luciana Marcondes, et al.FEBS Letters|March 12, 2004
Short interfering RNA-mediated gene targeting in the zebrafishAndrew Dodd, Stephen P Chambers, Donald R LoveSultan Qaboos University Medical Journal|April 11, 2013
Molecular Analysis of a Case of Thanatophoric Dysplasia Reveals Two de novo FGFR3 Missense Mutations located in cisRenate Marquis-Nicholson, Salim Aftimos, Donald R LoveAdvances in Bioinformatics|June 18, 2016
Evaluation of Bioinformatic Programmes for the Analysis of Variants within Splice Site Consensus RegionsRongying Tang, Debra O Prosser, Donald R LoveDrug Discovery Today. Technologies|July 2, 2014
Global gene expression analysis in the zebrafish: the challenge and the promiseFranz B Pichler, Andrew Dodd, Donald R LoveJournal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 8, 2015
Merosin-deficient congenital muscular dystrophy: A novel homozygous mutation in the laminin-2 geneClinton Turner, Rachael Mein, Cynthia Sharpe, et al.Expert Review of Gastroenterology & Hepatology|October 13, 2009
Role of gut microbiota in Crohn's diseasePhillip I Baker, Donald R Love, Lynnette R FergusonSultan Qaboos University Medical Journal|June 9, 2015
Predicting the Pathogenic Potential of BRCA1 and BRCA2 Gene Variants Identified in Clinical Genetic TestingClare Brookes, Stella Lai, Elaine Doherty, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 3, 2014
The New Zealand Neuromuscular Disease Registry: rate of diagnoses confirmed by molecular testingMiriam Rodrigues, Alexa Kidd, Donald R Love, et al.Heart, Lung & Circulation|June 6, 2016
Update on the Diagnosis and Management of Familial Long QT SyndromeKathryn E Waddell-Smith, Jonathan R Skinner, Pageof 19