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International Journal of Oncology|June 18, 2004
Molecular analysis of an immature ovarian teratoma with gliomatosis peritonei and recurrence suggests genetic independence of multiple tumorsD Hunter Best, Genelle M Butz, Karen Moller, et al.The Canadian Journal of Cardiology|April 4, 2015
When to offer genetic testing for pulmonary arterial hypertensionWendy K Chung, Eric D Austin, D Hunter Best, et al.Cardiology in the Young|July 16, 2015
Infantile pulmonary capillary haemangiomatosis: a lethal form of pulmonary hypertensionEiméar McGovern, Paul McNally, Maureen O'Sullivan, et al.Journal of Medical Genetics|March 8, 2011
Mosaic ACVRL1 and ENG mutations in hereditary haemorrhagic telangiectasia patientsD Hunter Best, Cecily Vaughn, Jamie McDonald, et al.Respiratory Medicine Case Reports|January 11, 2017
Pulmonary veno-occlusive disease: Two children with gradual disease progressionRonald W Day, Parker W Clement, Aimee O Hersh, et al.Journal of Clinical Bioinformatics|January 25, 2013
Cystic fibrosis testing in a referral laboratory: results and lessons from a six-year periodPerry G Ridge, Christine Miller, Pinar Bayrak-Toydemir, et al.NPJ Genomic Medicine|July 16, 2021
Effective variant filtering and expected candidate variant yield in studies of rare human diseaseBrent S Pedersen, Joe M Brown, Harriet Dashnow, et al.Journal of Clinical and Translational Science|December 1, 2021
Addressing ethical and laboratory challenges for initiation of a rapid whole genome sequencing programSabrina Malone Jenkins, Rachel Palmquist, Ashley L Kapron, et al.Chest|November 26, 2016
EIF2AK4 Mutations in Patients Diagnosed With Pulmonary Arterial HypertensionD Hunter Best, Kelli L Sumner, Benjamin P Smith, et al.The Journal of Molecular Diagnostics : JMD|July 15, 2014
Noncontinuously binding loop-out primers for avoiding problematic DNA sequences in PCR and sanger sequencingKelli Sumner, Jeffrey J Swensen, Melinda Procter, et al.Pageof 3