Case Reports
doi: 10.1002/ajmg.a.36242.
Epub 2013 Dec 5.
SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot
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- PMID: 24311514
- DOI: 10.1002/ajmg.a.36242
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Case Reports
SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot
Am J Med Genet A.
2014 Feb.
No abstract available
Comment in
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7p22.3 microdeletion disrupting SNX8 in a patient presenting with intellectual disability but no tetralogy of Fallot.Am J Med Genet A. 2014 Aug;164A(8):2133-5. doi: 10.1002/ajmg.a.36566. Epub 2014 Apr 8. Am J Med Genet A. 2014. PMID: 24715298 No abstract available.
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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.
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7p22.3 microdeletion disrupting SNX8 in a patient presenting with intellectual disability but no tetralogy of Fallot.Am J Med Genet A. 2014 Aug;164A(8):2133-5. doi: 10.1002/ajmg.a.36566. Epub 2014 Apr 8. Am J Med Genet A. 2014. PMID: 24715298 No abstract available.
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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.
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