DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Lo Nigro C, Chong CS, Smith AC, Dobyns WB, Carrozzo R, Ledbetter DH.
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome.
Hum Mol Genet 1997;
6 (02) 157-164
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