Communicating new knowledge on previously reported genetic variants

ανά Aronson, Samuel J., Clark, Eugene H., Varugheese, Matthew, Baxter, Samantha, Babb, Lawrence J., Rehm, Heidi L.
Έκδοση 2012

A novel clinician interface to improve clinician access to up-to-date genetic results

ανά Wilcox, Allison R, Neri, Pamela M, Volk, Lynn A, Newmark, Lisa P, Clark, Eugene H, Babb, Lawrence J, Varugheese, Matthew, Aronson, Samuel J, Rehm, Heidi L, Bates, David W
Έκδοση 2014

The GeneInsight Suite: A Platform to Support Laboratory and Provider Use of DNA based Genetic Testing

ανά Aronson, Samuel J., Clark, Eugene H., Babb, Lawrence J, Baxter, Samantha, Farwell, Lisa M., Funke, Birgit H., Hernandez, Amy Lovelette, Joshi, Victoria A., Lyon, Elaine, Parthum, Andrew R., Russell, Franklin J., Varugheese, Matthew, Venman, Thomas C., Rehm, Heidi L.
Έκδοση 2011

Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings

ανά Lubin, Ira M., Aziz, Nazneen, Babb, Lawrence J., Ballinger, Dennis, Bisht, Himani, Church, Deanna M., Cordes, Shaun, Eilbeck, Karen, Hyland, Fiona, Kalman, Lisa, Landrum, Melissa, Lockhart, Edward R., Maglott, Donna, Marth, Gabor, Pfeifer, John D., Rehm, Heidi L., Roy, Somak, Tezak, Zivana, Truty, Rebecca, Ullman-Cullere, Mollie, Voelkerding, Karl V., Worthey, Elizabeth A., Zaranek, Alexander W., Zook, Justin M.
Τόπος έκδοσης J Mol Diagn (2017)