DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Rendu J, Satre V, Testard H. et al.
7p22.3 microdeletion disrupting SNX8 in a patient presenting with intellectual disability but no tetralogy of Fallot.
Am J Med Genet A 2014;
164A (08) 2133-2135
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