Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX ( XLIS ) or LIS1

By Pilz Daniela T.  

Human Molecular Genetics, Vol. 8, Iss. 9, 1999-09 ,pp. : 1757-1760

Oxford University Press

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Point Mutations and an Intragenic Deletion in LIS1 , the Lissencephaly Causative Gene in Isolated Lissencephaly Sequence and Miller-Dieker Syndrome

By Lo Nigro Cristiana   Chong Samuel S.   Smith Ann C. M.   Dobyns William B.   Carrozzo Romeo   Ledbetter David H.  

Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 157-164

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

By Cardoso Carlos  

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

Oxford University Press

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Interaction between LIS1 and doublecortin, two lissencephaly gene products

By Caspi Michal   Atlas Roee   Kantor Ayelet   Sapir Tamar   Reiner Orly  

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

Oxford University Press

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TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins

By Kumar Ravinesh A.   Pilz Daniela T.   Babatz Timothy D.   Cushion Thomas D.   Harvey Kirsten   Topf Maya   Yates Laura   Robb Stephanie   Uyanik Gkhan   Mancini Gracia M.S.   Rees Mark I.   Harvey Robert J.   Dobyns William B.  

Human Molecular Genetics, Vol. 19, Iss. 14, 2010-07 ,pp. : 2817-2827

Oxford University Press

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