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Further Associations of Congenital Heart Disease and Genetic Syndromes: Report of a Case of Tetralogy of Fallot and Fabry’s Disease

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References

  1. Desnick RJ, Ioannou YA, Eng CM (1995) α-Galactosidase A deficiency: Fabry disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D, (eds) The Metabolic and Molecular Bases of Inherited Disease, 7th edn, Vol. 2. McGraw-Hill, New York, pp 2741–2784

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  2. Ferrans VJ, Hibbs RG, Burda CD (1969) The heart in Fabry’s disease: a histochemical and electron microscopic study. Am J Cardiol 24: 95–110

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Authors and Affiliations

  1. The Lillie Frank Abercrombie Section of Pediatric Cardiology Department of Pediatrics, Baylor College of Medicine and Texas Chidren’s Hospital, Houston, Texas

    Mark B. Lewin, John Belmont, Dan G. McNamara, G. Wesley Vick & Jeffrey A. Towbin

  2. The Department of Molecular and Human Genetics, Baylor College of Medicine and Texas Chidren’s Hospital, Houston, Texas

    Mark B. Lewin, John Belmont, Dan G. McNamara, G. Wesley Vick & Jeffrey A. Towbin

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  1. Mark B. Lewin
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  2. John Belmont
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  3. Dan G. McNamara
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  4. G. Wesley Vick
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  5. Jeffrey A. Towbin
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Lewin, M.B., Belmont, J., McNamara, D.G. et al. Further Associations of Congenital Heart Disease and Genetic Syndromes: Report of a Case of Tetralogy of Fallot and Fabry’s Disease. Pediatr Cardiol 20, 236–237 (1999). https://doi.org/10.1007/s002469900452

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  • DOI: https://doi.org/10.1007/s002469900452

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