| 1 | ICHD, JAG1
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| Silencing mutations in JAG1 gene may play crucial roles in the pathogenesis of Tetralogy of Fallot.
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| Safari-Arababadi A, Behjati-Ardakani M, Kalantar SM, Jaafarinia M.
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| Cell Mol Biol (Noisy-le-grand) 64(4):103-107. 2018
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| 2 | CSX, CTHM1, DEL22Q11, ICHD, JAG1, NKX2-5, TBX1, TRI21
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| Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.
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| Rauch R, Hofbeck M, Zweier C, Koch A, Zink S, Trautmann U, Hoyer J, Kaulitz R, Singer H, Rauch A.
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| J Med Genet 47(5):321-31. Epub 2009 Nov 30.PMID: 19948535 2010
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| 3 | ASD2, ASD3, GATA4, ICHD, JAG1, MYH6, NKX2-5, NOTCH1, TBX1, TBX20, TBX5, TFAP2B, THRAP2
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| The developmental genetics of congenital heart disease.
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| Bruneau BG.
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| Nature 451(7181):943-8. 2008
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| 4 | NOTCH1, NOTCH2, NOTCH3, JAG1, ICHD, PSEN1, PSEN2
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| The multifaceted role of Notch in cardiac development and disease.
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| High FA, Epstein JA.
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| Nat Rev Genet 9(1):49-61. Review. 2008
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| 5 | JAG1, ICHD
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| Conditional JAG1 mutation shows the developing heart is more sensitive than developing liver to JAG1 dosage.
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| Lu F, Morrissette JJ, Spinner NB.
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| Am J Hum Genet 72(4):1065-70. Epub 2003 Mar 14. 2003
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| 6 | JAG1, ICHD
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| Familial Tetralogy of Fallot caused by mutation in the jagged1 gene.
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| Eldadah ZA, Hamosh A, Biery NJ, Montgomery RA, Duke M, Elkins R, Dietz HC.
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| Hum Mol Genet 10(2):163-9. 2001
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