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Current Publications
We are dedicated to promoting academic initiatives through scientific and medical research. Thanks to our vast experience in the fields of genetics and oncology, our publications and presentations have made a significant positive impact on medical professionals and their patients.
Below is a listing of our most recent publications and presentations. Please review our Listing of All Publications for materials from previous years.
2008 Posters and Publications (PDF format)
Prevalence and instability of Fragile X alleles: Implications for Offering Fragile X Prenatal Diagnosis.
Cronister, A; Teicher, J; Rohlfs, EM; Donnenfeld, AE; Hallam S, Obstetrics and Gynecology 2008;111:596-601.
Consensus Characterization of 16 FMR1 Reference Materials: A Consortium Study
Jean Amos Eilson, Victoria M. Pratt, Amit Phansalkar, Kasinathan Muralidharan, W. Edeard Highsmith Jr., Jeanne C Beck, Scott Bridgeman, Ebony M. Courtney, Lidia Epp, Andrea Ferreira-Gonzalez, Nick L. Hjelm, Leonard M. Holtegaard, Mohamed A. Jama, John P. Jakupciak, Monique A. Johnson, Paul Labrousse, Elaine Lyon, Thomas W. Prior, C. Sue Richards, Kristy L. Richie, Benjamin B. Roa, Elizabeth M. Rohlfs, Tina Sellers, Stephanie L. Sherman, Karen A. Siegrist, Lawrence M. Silverman, Loanna Wiszniewska, Lisa V. Kalman and the Fragile Experts Working Group of the Association for Molecular Pathology Clinical Practice Committee, Journal of Molecular Diagnostics, Vol 10, No 1, January 2008
Multiple Rare Nonsynonymous Variants in the Adenomatous Polyposis Coli Gene Predispose to Colorectal Adenomas
Azzopardi, Duncan1; Dallosoo, Anothony R1; Eliason, Kristilyn3; Hendrickson, Brant C4; Jones, Natalie1; Rawstorne, Edward1; Colley1; James, Moskvina2; Valentina; Frye, Cynthia3; Sampson, Julian R1; Wenstrup, Richard3; Scholl, Thomas3,4; and Cheadle, Jeremy P.1
1Institute of Medical Genetics and 2Biostatistics and Bioinformatics Unit, School of Medicine, Cardiff University, Heath Park, Cardiff, United Kingdom; 3Myriad Genetic Laboratories, Inc., Salt Lake City, Utah; and 4Genzyme Genetics, Westborough, MA, Cancer Res 2008; 68: (2). January 15, 2008 pp358-363
Two cases assessed for myloid disorders had an unexpected twist
Reddy, Kavita, Cancer Genetics and Cytogenetics 181 (2008) 138-140 (Letter to the editor)
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