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

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Interaction between hamartin and tuberin, the TSC1 and TSC2 gene products

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Human Molecular Genetics, Vol. 7, Iss. 6, 1998-06 ,pp. : 1053-1057

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LIS1 and XLIS ( DCX ) mutations cause most classical lissencephaly, but different patterns of malformation

By Barkovich A.J.  

Human Molecular Genetics, Vol. 7, Iss. 13, 1998-12 ,pp. : 2029-2037

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Genetic and physical interaction between the NPHP5 and NPHP6 gene products

By Schfer Tobias   Ptz Michael   Lienkamp Soeren   Ganner Athina   Bergbreiter Astrid   Ramachandran Haribaskar   Gieloff Verena   Gerner Martin   Mattonet Christian   Czarnecki Peter G.   Sayer John A.   Otto Edgar A.   Hildebrandt Friedhelm   Kramer-Zucker Albrecht   Walz Gerd  

Human Molecular Genetics, Vol. 18, Iss. 21, 2009-11 ,pp. : 4226-4226

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