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References
Jerome LA, Papaioannou VE. DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1. Nat Genet 2001;27:286–291.
Benson DW, Sharkey A, Fatkin D, et al. Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects. Circulation 1998;97:2043–2048.
Musante L, Kehl HG, Majewski F, et al. Spectrum of mutations in PTPN11 and genotype-phenotype correlation in 96 patients with Noonan syndrome and five patients with cardiofacio-cutaneous syndrome. Eur J Hum Genet 2003;11:201–206.
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Milewicz, D.M. (2007). Genetic Aspects of Congenital Heart Disease. In: Willerson, J.T., Wellens, H.J.J., Cohn, J.N., Holmes, D.R. (eds) Cardiovascular Medicine. Springer, London. https://doi.org/10.1007/978-1-84628-715-2_127
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DOI: https://doi.org/10.1007/978-1-84628-715-2_127
Publisher Name: Springer, London
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