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| 1 | A gain-of-function TBX5 mutation is associated with atypical Holt Oram syndrome and paroxysmal atrial fibrillation显示文摘 | Postma AV van de Meerakker JB Mathijssen IB | 2008 | Circ Res2008，102，11： | 1 |
| 2 | Genomic organisation and chromosomal localisation of two members of the KCND ion channel family,KCND2 and KCND3显示文摘 | Postma AV Bezzina CR Vries JF D | 2000 | Hum Genet2000，106，6： | 1 |
| 3 | Absence of calsequestrin- 2 causes severe forms of catechelaminergic polymorphic ventricular tachycardia显示文摘 | Postma AV Denjoy I Hoorntje TM | 2002 | Circ Res2002，91，8： | 1 |
| 4 | Catecholaminergie polymorphic ventricular tachycardia:RYR2 mutations,bradycardia,and follow up of the patients显示文摘 | Postma AV Denjoy I Kamblock J | 2005 | J Med Genet2005，42，11： | 1 |
| 5 | Developmental and genetic aspects of atrial fibrillation 显示文摘 | Postma AV Dekker LR Soufan AT | 2009 | Trends Cardiovasc Med2009，19，： | 1 |
| 6 | Catecholaminergic polymorphicventricular tachycardia:RYR2 mutations,bradycardia,and follow up ofthe patients显示文摘 | Postma AV Denjoy I Kamblock J | 2005 | J Med Genet2005，42，： | 1 |
| 7 | Catecholaminergic polymorphic ventricular tachycardia:RYR2 mutations,bradycardia,and follow up of the patients显示文摘 | Postma AV Denjoy I Kamblock J | 2005 | Journal of medical genetics2005，42，11： | 1 |
| 8 | Absense of calsequestrin 2 causes severe forms of catecholaminergic polymorohic ventricular tachycardia显示文摘 | Postma AV Denjoy I Hoorntje TM | 2002 | Circ Res2002，91，： | 1 |
| 9 | Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia显示文摘 | Postma AV Denjoy I Hoorntje TM | 2002 | Circ Res2002，91，： | 1 |
| 10 | Absence of calsequeslrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia显示文摘 | Postma AV Denjoy I Hoomtje TM | 2002 | Circ Res2002，91，8： | 1 |
| 11 | A gain-of- function TBX5 mutation is associated with atypical Holt-Oram syn- drome and paroxysmal atrial fibrillation 显示文摘 | Postma AV van de Meerakker JB Mathijssen IB | 2008 | Cire Res2008，102，11： | 1 |
| 12 | Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia显示文摘 | Postma AV Denjoy I Hoorntje TM | 2002 | Circ Res2002，91，8： | 1 |
| 13 | A case of catecholaminergic polymorphic ventricular tachycardia caused by two calsequestrin 2 mutations显示文摘 | de la Fuente S van Langen IM Postma AV | 2008 | Pacing Clin Electrophysiol2008，31，7： | 1 |
| 14 | Catecholaminergic polymorphic ventricular tachycardia:RYR2 mutations,bradycardia,and follow up of the patients显示文摘 | Postma AV Denjoy I Kamblock J | 2005 | J Med Genet2005，42，11： | 1 |
| 15 | Ebstein anomaly associated with eft ventricular noncompaction:an autosomal dominant condition that can be caused by mutations in MYH7 显示文摘 | Vermeer AM van Engelen K Postma AV | 2013 | Am J Med Genet C Semin Med Genet2013，163，： | 1 |
| 16 | A gain-of-function TBX5 mutation is associated with atypical hoh-oram syndrome and paroxysmal atrial fibrillation显示文摘 | Postma AV van de Meerakker JBA Mathijssen IB | 2008 | Circ Res2008，102，： | 1 |
| 17 | Mutations in the sar- comere gene MYH7 in Ebstein anomaly显示文摘 | Postma AV van Engelen K van de Meerakker J | 2011 | Circ Cardiovasc Genet2011，4，： | 1 |
| 18 | 显示文摘 | Postma AV Denjoy I Hoomtje TM | 2002 | Circ Res2002，91，： | 1 |
| 19 | Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, brad- ycardia, and follow up of the patients显示文摘 | Postma AV Denjoy I Kamblock J | 2005 | J Med Genet2005，42，11： | 1 |
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