DOI:
10.1055/s-00029025
Journal of Pediatric Epilepsy
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References
Chatron N, Thibault L, Lespinasse J. et al.
Genetic counselling pitfall: co-occurrence of an 11.8-Mb Xp22 duplication and an Xp21.2 duplication disrupting IL1RAPL1.
Mol Syndromol 2017;
8 (06) 325-330
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