DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Jezela-Stanek A, Kucharczyk M, Falana K. , et al.
Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion encompassing NFIX gene and novel NFIX sequence variant.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 2016;
160 (01) 161-167
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