Results
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Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients. [electronic resource] by
- Postma, A V
- Denjoy, I
- Kamblock, J
- Alders, M
- Lupoglazoff, J-M
- Vaksmann, G
- Dubosq-Bidot, L
- Sebillon, P
- Mannens, M M A M
- Guicheney, P
- Wilde, A A M
Producer: 20060717
In:
Journal of medical genetics vol. 42
Availability: No items available.
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A single Na(+) channel mutation causing both long-QT and Brugada syndromes. [electronic resource] by
- Bezzina, C
- Veldkamp, M W
- van Den Berg, M P
- Postma, A V
- Rook, M B
- Viersma, J W
- van Langen, I M
- Tan-Sindhunata, G
- Bink-Boelkens, M T
- van Der Hout, A H
- Mannens, M M
- Wilde, A A
Producer: 20000104
In:
Circulation research vol. 85
Availability: No items available.
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4.
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Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal. [electronic resource] by
- Postma, A V
- Alders, M
- Sylva, M
- Bilardo, C M
- Pajkrt, E
- van Rijn, R R
- Schulte-Merker, S
- Bulk, S
- Stefanovic, S
- Ilgun, A
- Barnett, P
- Mannens, M M A M
- Moorman, A F M
- Oostra, R J
- van Maarle, M C
Producer: 20140908
In:
Journal of medical genetics vol. 51
Availability: No items available.
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Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7. [electronic resource] by
- van Engelen, K
- Postma, A V
- van de Meerakker, J B A
- Roos-Hesselink, J W
- Helderman-van den Enden, A T J M
- Vliegen, H W
- Rahman, T
- Baars, M J H
- Sels, J-W
- Bauer, U
- Pickardt, T
- Sperling, S R
- Moorman, A F M
- Keavney, B
- Goodship, J
- Klaassen, S
- Mulder, B J M
Producer: 20130225
In:
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation vol. 21
Availability: No items available.
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