Clinical genetics

Citations 331-340 of 397 total displayed.

Past content (since Feb 1999):

Clinical Investigations and Reports
Familial Thoracic Aortic Aneurysms and Dissections : Genetic Heterogeneity With a Major Locus Mapping to 5q13-14

Dongchuan Guo, Sumera Hasham, Shao-Qing Kuang, Carl J. Vaughan, Eric Boerwinkle, Hua Chen, Dianne Abuelo, Harry C. Dietz, Craig T. Basson, Sanjay S. Shete, and Dianna M. Milewicz
Circulation 2001;103:2461-2468 [Abstract] [Full text]  

Clinical Investigations and Reports
Identification of a Chromosome 11q23.2-q24 Locus for Familial Aortic Aneurysm Disease, a Genetically Heterogeneous Disorder

Carl J. Vaughan, Mairead Casey, Jie He, Mark Veugelers, Kiersten Henderson, Dongchuan Guo, Robert Campagna, Mary J. Roman, Dianna M. Milewicz, Richard B. Devereux, and Craig T. Basson
Circulation 2001;103:2469-2475 [Abstract] [Full text]  

Clinical Investigations and Reports
Premature Atherosclerosis Associated With Monogenic Insulin Resistance

Robert A. Hegele
Circulation 2001;103:2225-2229 [Abstract] [Full text]  

Clinical Investigations and Reports
Pharmacogenetic Interactions Between ß-Blocker Therapy and the Angiotensin-Converting Enzyme Deletion Polymorphism in Patients With Congestive Heart Failure

Dennis M. McNamara, Richard Holubkov, Karen Janosko, Amy Palmer, Jue J. Wang, Guy A. MacGowan, Srinivas Murali, Warren D. Rosenblum, Barry London, and Arthur M. Feldman
Circulation 2001;103:1644-1648 [Abstract] [Full text]  

Editorials
Adrenergic Receptor Polymorphisms and Cardiac Function (and Dysfunction) : A Failure to Communicate?

Ross D. Feldman
Circulation 2001;103:1042-1043 [Full text]  

Brief Rapid Communications
Blunted Cardiac Responses to Receptor Activation in Subjects With Thr164Ile ß₂-Adrenoceptors

Otto-Erich Brodde, Rainer Büscher, Ralph Tellkamp, Joachim Radke, Stefan Dhein, and Paul A. Insel
Circulation 2001;103:1048-1050 [Abstract] [Full text]  

Clinical Investigations and Reports
Notched T Waves on Holter Recordings Enhance Detection of Patients With LQT2 (HERG) Mutations

J. M. Lupoglazoff, I. Denjoy, M. Berthet, N. Neyroud, L. Demay, P. Richard, B. Hainque, G. Vaksmann, D. Klug, A. Leenhardt, G. Maillard, P. Coumel, and P. Guicheney
Circulation 2001;103:1095-1101 [Abstract] [Full text]  

Correspondence
Platelet Glycoprotein IIIa Pl^A Polymorphism and Effects of Aspirin on Thrombin Generation • Response

Andrzej Szczeklik, Marek Sanak, Anetta Undas, Paul F. Bray, Pascal Goldschmidt-Clermont, Mark I. Furman, Alan D. Michelson, Marc R. Barnard, Mary Ann Mascelli, Craig Hendrix, Lindsay Coleman, Jeanette Hamlington, Thomas Kickler, Douglas J. Christie, and Sourav Kundu
Circulation 2001;103:e33-34e [Full text]  

Correspondence
Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement • Response

Hartmut H.-J. Schmidt, Herbert Lochs, Gary L. Brodsky, Luisa Mestroni, Francesco Muntoni, Caroline Sewry, Snjezana Miocic, and Gianfranco Sinagra
Circulation 2001;103:e20 [Full text]  

Clinical Investigations and Reports
Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia

Päivi J. Laitinen, Kevin M. Brown, Kirsi Piippo, Heikki Swan, Joe M. Devaney, Bhoomi Brahmbhatt, Elizabeth A. Donarum, Michael Marino, Natascia Tiso, Matti Viitasalo, Lauri Toivonen, Dietrich A. Stephan, and Kimmo Kontula
Circulation 2001;103:485-490 [Abstract] [Full text]  

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