DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Romeo A, Lodi M, Viri M. , et al.
Does the co-occurrence of FGFR3 gene mutation in hypochondroplasia, medial temporal lobe dysgenesis, and focal epilepsy suggest a syndrome?.
Pediatr Neurol 2014;
50 (04) 427-430
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