Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome.
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D. Ledbetter | W. Dobyns | S. Chong | R. Carrozzo | Ann C M Smith | C. Lo Nigro | C. Nigro | A. Smith | C. S. Chong | A. Smith | C. L. Nigro