نتائج البحث - Basran, Raveen

An Update on Molecular Diagnostic Testing of Human Imprinting Disorders حسب Grafodatskaya, Daria, Choufani, Sanaa, Basran, Raveen, Weksberg, Rosanna

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A Next-Generation Sequencing Primer—How Does It Work and What Can It Do? حسب Alekseyev, Yuriy O., Fazeli, Roghayeh, Yang, Shi, Basran, Raveen, Maher, Thomas, Miller, Nancy S., Remick, Daniel

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Wilms tumour in Beckwith–Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines حسب Brzezinski, Jack, Shuman, Cheryl, Choufani, Sanaa, Ray, Peter, Stavropoulos, Dmitiri J, Basran, Raveen, Steele, Leslie, Parkinson, Nicole, Grant, Ronald, Thorner, Paul, Lorenzo, Armando, Weksberg, Rosanna

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Reply to Brioude et al حسب Brzezinski, Jack, Shuman, Cheryl, Choufani, Sanaa, Ray, Peter, Stavropoulos, Dimitri J, Basran, Raveen, Steele, Leslie, Parkinson, Nicole, Grant, Ronald, Thorner, Paul, Lorenzo, Armando, Weksberg, Rosanna

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A T-to-G Transversion at Nucleotide −567 Upstream of HBG2 in a GATA-1 Binding Motif Is Associated with Elevated Hemoglobin F حسب Chen, Zhiyi, Luo, Hong-Yuan, Basran, Raveen K., Hsu, Tien-Huei, Mang, Daniel W. H., Nuntakarn, Lalana, Rosenfield, Cathy G., Patrinos, George P., Hardison, Ross C., Steinberg, Martin H., Chui, David H. K.

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Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study حسب Cohn, Iris, Paton, Tara A., Marshall, Christian R., Basran, Raveen, Stavropoulos, Dimitri J., Ray, Peter N., Monfared, Nasim, Hayeems, Robin Z., Meyn, M. Stephen, Bowdin, Sarah, Scherer, Stephen W., Cohn, Ronald D., Ito, Shinya

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Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray حسب Hayeems, Robin Z., Bhawra, Jasmin, Tsiplova, Kate, Meyn, M. Stephen, Monfared, Nasim, Bowdin, Sarah, Stavropoulos, D. James, Marshall, Christian R., Basran, Raveen, Shuman, Cheryl, Ito, Shinya, Cohn, Iris, Hum, Courtney, Girdea, Marta, Brudno, Michael, Cohn, Ronald D., Scherer, Stephen W., Ungar, Wendy J.

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CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions حسب Butcher, Darci T., Cytrynbaum, Cheryl, Turinsky, Andrei L., Siu, Michelle T., Inbar-Feigenberg, Michal, Mendoza-Londono, Roberto, Chitayat, David, Walker, Susan, Machado, Jerry, Caluseriu, Oana, Dupuis, Lucie, Grafodatskaya, Daria, Reardon, William, Gilbert-Dussardier, Brigitte, Verloes, Alain, Bilan, Frederic, Milunsky, Jeff M., Basran, Raveen, Papsin, Blake, Stockley, Tracy L., Scherer, Stephen W., Choufani, Sanaa, Brudno, Michael, Weksberg, Rosanna

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Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test حسب Lionel, Anath C, Costain, Gregory, Monfared, Nasim, Walker, Susan, Reuter, Miriam S, Hosseini, S Mohsen, Thiruvahindrapuram, Bhooma, Merico, Daniele, Jobling, Rebekah, Nalpathamkalam, Thomas, Pellecchia, Giovanna, Sung, Wilson W L, Wang, Zhuozhi, Bikangaga, Peter, Boelman, Cyrus, Carter, Melissa T, Cordeiro, Dawn, Cytrynbaum, Cheryl, Dell, Sharon D, Dhir, Priya, Dowling, James J, Heon, Elise, Hewson, Stacy, Hiraki, Linda, Inbar-Feigenberg, Michal, Klatt, Regan, Kronick, Jonathan, Laxer, Ronald M, Licht, Christoph, MacDonald, Heather, Mercimek-Andrews, Saadet, Mendoza-Londono, Roberto, Piscione, Tino, Schneider, Rayfel, Schulze, Andreas, Silverman, Earl, Siriwardena, Komudi, Snead, O Carter, Sondheimer, Neal, Sutherland, Joanne, Vincent, Ajoy, Wasserman, Jonathan D, Weksberg, Rosanna, Shuman, Cheryl, Carew, Chris, Szego, Michael J, Hayeems, Robin Z, Basran, Raveen, Stavropoulos, Dimitri J, Ray, Peter N, Bowdin, Sarah, Meyn, M Stephen, Cohn, Ronald D, Scherer, Stephen W, Marshall, Christian R

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