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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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17.
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Exclusion of HRAS from long QT locus. [electronic resource] by
- Roy, N
- Kahlem, P
- Dausse, E
- Bennaceur, M
- Fauré, S
- Weissenbach, J
- Komajda, M
- Denjoy, I
- Coumel, P
- Schwartz, K
Producer: 19950309
In:
Nature genetics vol. 8
Availability: No items available.
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18.
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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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Evaluation of in-stent restenosis in proximal coronary arteries with multidetector computed tomography (MDCT). [electronic resource] by
- Chabbert, V
- Carrie, D
- Bennaceur, M
- Maupas, E
- Lauwers, V
- Mhem, M
- Lhermusier, T
- Elbaz, M
- Joffre, F
- Rousseau, H
- Puel, J
Producer: 20070913
In:
European radiology vol. 17
Availability: No items available.
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20.
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Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene. [electronic resource] by
- Charron, P
- Dubourg, O
- Desnos, M
- Bennaceur, M
- Carrier, L
- Camproux, A C
- Isnard, R
- Hagege, A
- Langlard, J M
- Bonne, G
- Richard, P
- Hainque, B
- Bouhour, J B
- Schwartz, K
- Komajda, M
Producer: 19980709
In:
Circulation vol. 97
Availability: No items available.
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