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Applied & Translational Genomics|June 14, 2016
Quality standards for DNA sequence variation databases to improve clinical management under development in AustraliaB Bennetts, M Caramins, A Hsu, et al.
World Journal of Surgery|January 9, 2015
Essential surgery: the way forwardJaymie Ang Henry, Chris Bem, Caris Grimes, et al.
Pediatric Nephrology (Berlin, Germany)|May 31, 2013
DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome, Judy Savige, Elisabet Ars, et al.
Journal of the American Academy of Dermatology|August 28, 2024
A randomized controlled trial analyzing nonthermal atmospheric plasma for the treatment of verruca vulgaris in pediatric patientsCourtney L Walker, Chelsea N Shope, Laura A Andrews, et al.
Pediatrics|June 1, 1989
Severity of disease correlated with fever reduction in febrile infantsR C Baker, T Tiller, J C Bausher, et al.
Human Mutation|November 14, 2008
Somatic mutation databases as tools for molecular epidemiology and molecular pathology of cancer: proposed guidelines for improving data collection, distribution, and integrationM Olivier, A Petitjean, J Teague, et al.
Human Mutation|March 24, 2009
Sharing data between LSDBs and central repositoriesJohan T den Dunnen, Rolf H Sijmons, Paal S Andersen, et al.
Neuroreport|May 9, 2002
Alternative transcripts of presenilin-1 associated with frontotemporal dementiaGeneviève Evin, Margaret J Smith, Angela Tziotis, et al.
Neuroreport|April 26, 2002
Alternative transcripts of presenilin-1 associated with frontotemporal dementiaGeneviève Evin, Margaret J Smith, Angela Tziotis, et al.
Brain Research. Molecular Brain Research|August 13, 2004
Expression of truncated presenilin 2 splice variant in Alzheimer's disease, bipolar disorder, and schizophrenia brain cortexMargaret J Smith, Robyn A Sharples, Geneviève Evin, et al.
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