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KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome. [electronic resource] by
- Donger, C
- Denjoy, I
- Berthet, M
- Neyroud, N
- Cruaud, C
- Bennaceur, M
- Chivoret, G
- Schwartz, K
- Coumel, P
- Guicheney, P
Producer: 19971212
In:
Circulation vol. 96
Availability: No items available.
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[T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)]. [electronic resource] by
- Lupoglazoff, J M
- Denjoy, I
- Berthet, M
- Hainque, B
- Vaksmann, G
- Klug, D
- Villain, E
- Lucet, V
- Guicheney, P
- Coumel, P
Producer: 20010719
In:
Archives des maladies du coeur et des vaisseaux vol. 94
Availability: No items available.
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A mutation in HERG associated with notched T waves in long QT syndrome. [electronic resource] by
- Dausse, E
- Berthet, M
- Denjoy, I
- André-Fouet, X
- Cruaud, C
- Bennaceur, M
- Fauré, S
- Coumel, P
- Schwartz, K
- Guicheney, P
Producer: 19970129
In:
Journal of molecular and cellular cardiology vol. 28
Availability: No items available.
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