Search Results - Deborah A. McDermott
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1
Mutation of Perinatal Myosin Heavy Chain Associated with a Carney Complex Variant by Mark Veugelers, Michael Bressan, Deborah A. McDermott, Stanislawa Weremowicz, Cynthia C. Morton, C. Charlton Mabry, Jean-François Lefaivre, Alan Zunamon, Anne Destrèe, Jean-Marie Chaudron, Craig T. Basson
Published 2004Artigo -
2
Relevance of Genetics and Genomics for Prevention and Treatment of Cardiovascular Disease by Donna K. Arnett, Alison E. Baird, Ruth Ann Barkley, Craig T. Basson, Eric Boerwinkle, Santhi K. Ganesh, David M. Herrington, Yuling Hong, Cashell E. Jaquish, Deborah A. McDermott, Christopher J. O’Donnell
Published 2007Artigo -
3
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy by Brenda Gerull, Arnd Heuser, Thomas Wichter, Matthias Paul, Craig T. Basson, Deborah A. McDermott, Bruce B. Lerman, Steve Markowitz, Patrick T. Ellinor, Calum A. MacRae, Stefan Peters, Katja S. Grossmann, Beate Michely, Sabine Klaassen, Walter Birchmeier, Rainer Dietz, Günter Breithardt, Eric Schulze‐Bahr, Ludwig Thierfelder
Published 2004Artigo -
4
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management by Angela E. Lin, Craig T. Basson, Elizabeth Goldmuntz, Pilar Magoulas, Deborah A. McDermott, Donna M. McDonald‐McGinn, Elspeth McPherson, Colleen A. Morris, Jacqueline A. Noonan, C. Nowak, Mary Ella Pierpont, Reed E. Pyeritz, Alan F. Rope, Elaine H. Zackai, Barbara R. Pober
Published 2008Revisão -
5
TBX5 Genetic Testing Validates Strict Clinical Criteria for Holt-Oram Syndrome by Deborah A. McDermott, Michael Bressan, Jié He, Joseph S. Lee, Salim Aftimos, Martina Brueckner, Fiona J. Gilbert, Gail E. Graham, Mark C. Hannibal, Jeffrey W. Innis, Mary Ella Pierpont, Annick Raas‐Rothschild, Alan Shanske, Wendy E. Smith, Robert H. Spencer, Martin G. St. John-Sutton, Lionel Van Maldergem, Darrel Waggoner, Matthew P. Weber, Craig T. Basson
Published 2005Artigo -
6
Genetics and Genomics for the Prevention and Treatment of Cardiovascular Disease: Update by Santhi K. Ganesh, Donna K. Arnett, Themistocles L. Assimes, Craig T. Basson, Aravinda Chakravarti, Patrick T. Ellinor, Mary B. Engler, Elizabeth Goldmuntz, David M. Herrington, Ray E. Hershberger, Yuling Hong, Julie A. Johnson, Steven J. Kittner, Deborah A. McDermott, James F. Meschia, Luisa Mestroni, Christopher J. O’Donnell, Bruce M. Psaty, Ramachandran S. Vasan, Marc Ruel, Win-Kuang Shen, André Terzic, Scott A. Waldman
Published 2013Artigo -
7
Comparative <i>PRKAR1A</i> genotype–phenotype analyses in humans with Carney complex and <i>prkar1a</i> haploinsufficient mice by Mark Veugelers, David Wilkes, Kimberly A. Burton, Deborah A. McDermott, Yan Song, Marsha M. Goldstein, Krista La Perle, Carl J. Vaughan, A.H. O'Hagan, Kenneth R. Bennett, Beat J. Meyer, Eric Legius, Mervi Karttunen, Reijo Norio, Helena Kääriäinen, Michael H. Lavyne, Jean-Philippe Neau, Gert Richter, Kaan Kırali, Alan Farnsworth, Karen Stapleton, P Morelli, Yoshinori Takanashi, J. Steven Bamforth, Franz Eitelberger, Irene Noszian, Waldimiro Manfroi, James C. Powers, Yoshihiko Mochizuki, Tsuneo Imai, Gary Ko, Deborah A. Driscoll, Elizabeth Goldmuntz, Jay M. Edelberg, Amanda Collins, Diana Eccles, Alan D. Irvine, G. Stanley McKnight, Craig T. Basson
Published 2004Artigo
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