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Clinical genetics
Citations 361-370 of 397 total displayed.
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Past content
(since Feb 1999):
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- Clinical Investigations and Reports
Deletion of a 5-cM Region at Chromosome 8p23 Is Associated With a Spectrum of Congenital Heart Defects
- Sabrina Giglio, Sharon L. Graw, Giorgio Gimelli, Barbara Pirola, Paolo Varone, Lucille Voullaire, Franco Lerzo, Elena Rossi, Claudia Dellavecchia, Maria Clara Bonaglia, Maria Cristina Digilio, Aldo Giannotti, Bruno Marino, Romeo Carrozzo, Julie R. Korenberg, Cesare Danesino, Eva Sujansky, Bruno Dallapiccola, and Orsetta Zuffardi
Circulation 2000;102:432-437
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- Clinical Investigations and Reports
Insertion/Deletion Polymorphism of the Angiotensin I-Converting Enzyme Gene Is Not Associated With Restenosis After Coronary Stent Placement
- Werner Koch, Adnan Kastrati, Julinda Mehilli, Corinna Böttiger, Nicolas von Beckerath, and Albert Schömig
Circulation 2000;102:197-202
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- Circulation Electronic Pages
The G20210A Prothrombin Mutation and the Physicians’ Health Study • Response
- Felicita Andreotti, Francesco Burzotta, Valerio De Stefano, Attilio Maseri, Licia Iacoviello, Paul M. Ridker, Charles H. Hennekens, and Joseph P. Miletich
Circulation 2000;101:e207-208e
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- Images in Cardiovascular Medicine
T-Wave Alternans Preceding Torsade de Pointes Ventricular Tachycardia
- Antonis A. Armoundas, Toshihiko Nanke, and Richard J. Cohen MD
Circulation 2000;101:2550
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- Circulation Electronic Pages
Holt-Oram Syndrome vs Heart-Hand Syndrome • Response
- Craig T. Basson, Thomas Münzel, Carsten Brockhoff, Henning Kober, Nikos Tsilimingas, Friedhelm Dapper, and Thomas Meinertz
Circulation 2000;101:e191
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- Clinical Investigations and Reports
Deletion Allele of Angiotensin-Converting Enzyme Gene Increases Risk of Essential Hypertension in Japanese Men : The Suita Study
- Jitsuo Higaki, Shunroku Baba, Tomohiro Katsuya, Noriyuki Sato, Kazuhiko Ishikawa, Toshihumi Mannami, Jun Ogata, and Toshio Ogihara
Circulation 2000;101:2060-2065
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- Clinical Investigations and Reports
Effects of Flecainide in Patients With New SCN5A Mutation : Mutation-Specific Therapy for Long-QT Syndrome?
- J. Benhorin, R. Taub, M. Goldmit, B. Kerem, R. S. Kass, I. Windman, and A. Medina
Circulation 2000;101:1698-1706
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- Clinical Investigations and Reports
Genetic Determinants of Hemostasis Phenotypes in Spanish Families
- Juan Carlos Souto, Laura Almasy, Montserrat Borrell, Merce Garí, Elisabet Martínez, José Mateo, William H. Stone, John Blangero, and Jordi Fontcuberta
Circulation 2000;101:1546-1551
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- Clinical Investigations and Reports
The Apolipoprotein  4 Allele Determines Prognosis and the Effect on Prognosis of Simvastatin in Survivors of Myocardial Infarction : A Substudy of the Scandinavian Simvastatin Survival Study
- Lars Ulrik Gerdes, Christian Gerdes, Kari Kervinen, Markku Savolainen, Ib Christian Klausen, Peter Steen Hansen, Y. Antero Kesäniemi, and Ole Færgeman
Circulation 2000;101:1366-1371
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- Clinical Investigations and Reports
Hypoxia-Induced Pulmonary Blood Redistribution in Subjects With a History of High-Altitude Pulmonary Edema
- Masayuki Hanaoka, Masao Tanaka, Ri-Li Ge, Yunden Droma, Atsuko Ito, Takashige Miyahara, Tomonobu Koizumi, Keisaku Fujimoto, Tadashige Fujii, Toshio Kobayashi, and Keishi Kubo
Circulation 2000;101:1418-1422
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