| 1 | DEL8P21, DEL8P23, GATA4, LVNC
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| Noncompaction of the left ventricular myocardium in a boy with a novel chromosome 8p23.1 deletion.
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| Blinder JJ, Martinez HR, Craigen WJ, Belmont J, Pignatelli RH, Jefferies JL.
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| Am J Med Genet A 155(9):2215-20. doi: 10.1002/ajmg.a.34129. Epub 2011 Aug 10. 2011
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| 2 | DEL1P36, LVNC
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| Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36.
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| Saito S, Kawamura R, Kosho T, Shimizu T, Aoyama K, Koike K, Wada T, Matsumoto N, Kato M, Wakui K, Fukushima Y.
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| Am J Med Genet A 146A(22):2891-2897. [Epub ahead of print] 2008
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| 3 | DEL1P36, LVNC
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| Left-ventricular non-compaction (LVNC): A clinical feature more often observed in terminal deletion 1p36 than previously expected.
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| Cremer K, Lüdecke HJ, Ruhr F, Wieczorek D.
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| Eur J Med Genet ur J Med Genet. 2008 Jul 31. [Epub ahead of print] 2008
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| 4 | DEL1P36, LVNC
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| Left-ventricular non-compaction in a patient with monosomy 1p36.
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| Thienpont B, Mertens L, Buyse G, Vermeesch JR, Devriendt K.
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| Eur J Med Genet 50(3):233-6. Epub 2007 Jan 27. 2007
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| 5 | TAZ, DTNA, INVM, LVNC
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| Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12.
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| Kenton AB, Sanchez X, Coveler KJ, Makar KA, Jimenez S, Ichida F, Murphy RT, Elliott PM, McKenna W, Bowles NE, Towbin JA, Bowles KR.
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| Mol Genet Metab 82(2):162-6. 2004
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| 6 | BTHS2, DTNA, BTHS, LVNC, TAZ
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| Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome.
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| Ichida F, Tsubata S, Bowles KR, Haneda N, Uese K, Miyawaki T, Dreyer WJ, Messina J, Li H, Bowles NE, Towbin JA.
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| Circulation 103(9):1256-63. 2001
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| 7 | DTNA, LVNC
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| Isolated noncompaction of the myocardium in adults.
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| Ritter M, Oechslin E, Sutsch G, Attenhofer C, Schneider J, Jenni R.
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| Mayo Clin Proc 72(1):26-31. 1997
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