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Clinical genetics
Citations 21-30 of 38 total displayed.
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Past content
(since Mar 2000):
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- Clinical Research
Chromosome 1q21.1 Contiguous Gene Deletion Is Associated With Congenital Heart Disease
- Jesse Christiansen, John D. Dyck, Basil G. Elyas, Margaret Lilley, J. Stephen Bamforth, Mark Hicks, Kathleen A. Sprysak, Robert Tomaszewski, Shelagh M. Haase, Leanne M. Vicen-Wyhony, and Martin J. Somerville
Circ. Res. 2004;94:1429-1435; published online before print as doi:10.1161/01.RES.0000130528.72330.5c
[Abstract]
[Full text]
- Articles
Chromosome 1q21.1 Contiguous Gene Deletion Is Associated With Congenital Heart Disease
- Jesse Christiansen, John D. Dyck, Basil G. Elyas, Margaret Lilley, J. Stephen Bamforth, Mark Hicks, Kathleen A. Sprysak, Robert Tomaszewski, Shelagh M. Haase, Leanne M. Vicen-Wyhony, and Martin J. Somerville
Circ. Res. published April 29, 2004, doi:10.1161/01.RES.0000130528.72330.5c
[Abstract]
- Integrative Physiology
Matrix Metalloproteinase-3 Genotype Contributes to Age-Related Aortic Stiffening Through Modulation of Gene and Protein Expression
- Tanya L. Medley, Bronwyn A. Kingwell, Christoph D. Gatzka, Prakash Pillay, and Timothy J. Cole
Circ. Res. 2003;92:1254-1261; published online before print as doi:10.1161/01.RES.0000076891.24317.CA
[Abstract]
[Full text]
- Articles
Matrix Metalloproteinase-3 Genotype Contributes to Age-Related Aortic Stiffening Through Modulation of Gene and Protein Expression
- Tanya L. Medley, Bronwyn A. Kingwell, Christoph D. Gatzka, Prakash Pillay, and Timothy J. Cole
Circ. Res. published May 15, 2003, doi:10.1161/01.RES.0000076891.24317.CA
[Abstract]
- Clinical Research
Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in the Conduction System
- Connie R. Bezzina, Martin B. Rook, W.Antoinette Groenewegen, Lucas J. Herfst, Allard C. van der Wal, Jan Lam, Habo J. Jongsma, Arthur A.M. Wilde, and Marcel M.A.M. Mannens
Circ. Res. 2003;92:159-168; published online before print as doi:10.1161/01.RES.0000052672.97759.36
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- Clinical Research
A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill
- W. Antoinette Groenewegen, Mehran Firouzi, Connie R. Bezzina, Saskia Vliex, Irene M. van Langen, Lodewijk Sandkuijl, Jeroen P.P. Smits, Miriam Hulsbeek, Martin B. Rook, Habo J. Jongsma, and Arthur A.M. Wilde
Circ. Res. 2003;92:14-22; published online before print as doi:10.1161/01.RES.0000050585.07097.D7
[Abstract]
[Full text]
- Articles
Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in the Conduction System
- Connie R. Bezzina, Martin B. Rook, W. Antoinette Groenewegen, Lucas J. Herfst, Allard C. van der Wal, Jan Lam, Habo J. Jongsma, Arthur A.M. Wilde, and Marcel M.A.M. Mannens
Circ. Res. published December 19, 2002, doi:10.1161/01.RES.0000052672.97759.36
[Abstract]
- Articles
Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill
- W. Antoinette Groenewegen, Mehran Firouzi, Connie R. Bezzina, Saskia Vliex, Irene M. van Langen, Lodewijk Sandkuijl, Jeroen P.P. Smits, Miriam Hulsbeek, Martin B. Rook, Habo J. Jongsma, and Arthur A.M. Wilde
Circ. Res. published December 5, 2002, doi:10.1161/01.RES.0000050585.07097.D7
[Abstract]
- Reviews
Development of the Coronary Vessel System
- David E. Reese, Takashi Mikawa, and David M. Bader
Circ. Res. 2002;91:761-768, doi:10.1161/01.RES.0000038961.53759.3C
[Abstract]
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- UltraRapid Communications
Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia
- Alex V. Postma, Isabelle Denjoy, Theo M. Hoorntje, Jean-Marc Lupoglazoff, Antoine Da Costa, Pascale Sebillon, Marcel M.A.M. Mannens, Arthur A.M. Wilde, and Pascale Guicheney
Circ. Res. 2002;91:e21-26e; published online before print as doi:10.1161/01.RES.0000038886.18992.6B
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