A Revision of the Lissencephaly and Miller-Dieker Syndrome Critical Regions in Chromosome 17p13.3

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Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 147-155

Oxford University Press

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The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene

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Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 3019-3028

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Interaction between LIS1 and doublecortin, two lissencephaly gene products

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Human Molecular Genetics, Vol. 9, Iss. 15, 2000-09 ,pp. : 2205-2213

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Isolation and embryonic expression of the novel mouse gene Hic1 , the homologue of HIC1 , a candidate gene for the Miller–Dieker syndrome

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Mice deficient in the candidate tumor suppressor gene Hic1 exhibit developmental defects of structures affected in the Miller–Dieker syndrome

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