نتائج البحث - Deborah A. McDermott
- يعرض 1 - 7 نتائج من 7
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Mutation of Perinatal Myosin Heavy Chain Associated with a Carney Complex Variant حسب 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
منشور في 2004Artigo -
2
Relevance of Genetics and Genomics for Prevention and Treatment of Cardiovascular Disease حسب 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
منشور في 2007Artigo -
3
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy حسب 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
منشور في 2004Artigo -
4
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management حسب 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
منشور في 2008Revisão -
5
TBX5 Genetic Testing Validates Strict Clinical Criteria for Holt-Oram Syndrome حسب 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
منشور في 2005Artigo -
6
Genetics and Genomics for the Prevention and Treatment of Cardiovascular Disease: Update حسب 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
منشور في 2013Artigo -
7
Comparative <i>PRKAR1A</i> genotype–phenotype analyses in humans with Carney complex and <i>prkar1a</i> haploinsufficient mice حسب 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
منشور في 2004Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Gene
Medicine
Internal medicine
Mutation
Bioinformatics
Cardiology
Carney complex
Disease
Environmental health
Genetic testing
Genotype
Intensive care medicine
Missense mutation
Pediatrics
Population
Psychiatry
Abnormality
Arrhythmogenic right ventricular dysplasia
Atrioventricular canal
Cancer research
Carcinogenesis
Cardiomyopathy
Catenin
Cell
Computational biology
Desmoplakin
Desmosome
Genetic counseling