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Correspondence regarding SNX8 haploinsufficiency and its potential for cardiac anomalies including tetralogy of Fallot.
Am J Med Genet A. 2014 Aug;164A(8):2136-7. doi: 10.1002/ajmg.a.36572. Epub 2014 Apr 14.
Am J Med Genet A. 2014.
PMID: 24733602
No abstract available.
SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot.
Vanzo RJ, Martin MM, Sdano MR, Teta K, Aggarwal V, South ST.
Vanzo RJ, et al. Among authors: teta k.
Am J Med Genet A. 2014 Feb;164A(2):554-6. doi: 10.1002/ajmg.a.36242. Epub 2013 Dec 5.
Am J Med Genet A. 2014.
PMID: 24311514
No abstract available.
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