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Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|September 27, 2002
Identifying and quantifying sources of variation in microarray data using high-density cDNA membrane arraysKevin R Coombes, W Edward Highsmith, Tammy A Krogmann, et al.Mayo Clinic Proceedings|August 11, 2018
A Patient With Hereditary ATTR and a Novel AGel p.Ala578Pro AmyloidosisMeera Sridharan, W Edward Highsmith, Paul J Kurtin, et al.The Journal of Molecular Diagnostics : JMD|January 26, 2007
Homozygous transthyretin mutation in an African American MaleEapen K Jacob, William D Edwards, Mark Zucker, et al.The Journal of Molecular Diagnostics : JMD|November 5, 2013
Homozygosity for the V122I mutation in transthyretin is associated with earlier onset of cardiac amyloidosis in the African American population in the seventh decade of lifeHoney V Reddi, Sarah Jenkins, Jason Theis, et al.Journal of Clinical Microbiology|July 1, 2016
Multicenter Evaluation of the Solana Group A Streptococcus Assay: Comparison with CultureTimothy S Uphoff, Blake W Buchan, Nathan A Ledeboer, et al.Plos One|November 28, 2012
A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophyEric D Wieben, Ross A Aleff, Nirubol Tosakulwong, et al.Journal of Child Neurology|December 26, 2012
Neurodevelopmental disabilities in children with intermediate and premutation range fragile X cytosine-guanine-guanine expansionsMeredith M Renda, Robert G Voigt, Dusica Babovic-Vuksanovic, et al.Cancer|November 4, 2009
Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations and risk for pancreatic adenocarcinomaRobert R McWilliams, Gloria M Petersen, Kari G Rabe, et al.Cold Spring Harbor Molecular Case Studies|January 31, 2019
Identification of aggressive Gardner syndrome phenotype associated with a de novo APC variant, c.4666dupPatrick Kiessling, Eric Dowling, Yajue Huang, et al.Molecular Genetics and Metabolism|May 4, 2010
Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencingEmily H Smith, Cheryl Thomas, David McHugh, et al.Pageof 8