Sökresultat - Carole Harris‐Kerr
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Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test av Jamie D. Kapplinger, David J. Tester, Benjamin A. Salisbury, Janet L. Carr, Carole Harris‐Kerr, Guido D. Pollevick, Arthur A.M. Wilde, Michael J. Ackerman
Publicerad 2009Artigo -
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Genetic Variation in the 6p22.3 Gene DTNBP1, the Human Ortholog of the Mouse Dysbindin Gene, Is Associated with Schizophrenia av Richard E. Straub, Yuxin Jiang, Charles J. MacLean, Yunlong Ma, Bradley T. Webb, Maxim V. Myakishev, Carole Harris‐Kerr, Brandon Wormley, Hannah Sadek, B Kadambi, Anthony J. Cesare, Avi Gibberman, Xu Wang, F. Anthony O’Neill, Dermot Walsh, Kenneth S. Kendler
Publicerad 2002Artigo -
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An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing av Jamie D. Kapplinger, David J. Tester, Mariëlle Alders, Begoña Benito, Myriam Berthet, Josép Brugada, Pedro Brugada, Véronique Fressart, Alejandra Guerchicoff, Carole Harris‐Kerr, Shiro Kamakura, Florence Kyndt, Tamara T. Koopmann, Yoshihiro Miyamoto, Ryan Pfeiffer, Guido D. Pollevick, Vincent Probst, Sven Zumhagen, Matteo Vatta, Jeffrey A. Towbin, Wataru Shimizu, Eric Schulze‐Bahr, Charles Antzelevitch, Benjamin A. Salisbury, Pascale Guicheney, Arthur A.M. Wilde, Ramón Brugada, Jean‐Jacques Schott, Michael J. Ackerman
Publicerad 2009Artigo
Sökverktyg:
Relaterade ämnen
Biology
Gene
Genetics
Genetic testing
Internal medicine
Medicine
Mutation
Genotype
Long QT syndrome
Missense mutation
QT interval
Allele
Anthropology
Brugada syndrome
Frameshift mutation
Genetic linkage
Haplotype
Linkage disequilibrium
Nuclear family
Pediatrics
Pedigree chart
Predictive testing
Proband
Short QT syndrome
Single-nucleotide polymorphism
Sociology