Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females

By Schachter S.C.  

Human Molecular Genetics, Vol. 10, Iss. 17, 2001-08 ,pp. : 1775-1783

Oxford University Press

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Linkage and Physical Mapping of X-Linked Lissencephaly/SBH ( XLIS ): A Gene Causing Neuronal Migration Defects in Human Brain

By Ross M. Elizabeth   Allen Kristina M.   Srivastava Anand K.   Featherstone Terry   Gleeson Joseph G.   Hirsch Betsy   Harding Brian N.   Andermann Eva   Abdullah Rabi   Berg Michael   Czapansky-Bielman Desireé   Flanders Dean J.   Guerrini Renzo   Motté Jacques   Mira A. Puche   Scheffer Ingrid   Berkovic Samuel   Scaravilli F.   King Richard A.   Ledbetter David H.   Schlessinger David   Dobyns William B.   Walsh Christopher A.  

Human Molecular Genetics, Vol. 6, Iss. 4, 1997-01 ,pp. : 555-562

Oxford University Press

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Human doublecortin ( DCX ) and the homologous gene in mouse encode a putative Ca 2+ -dependent signaling protein which is mutated in human X-linked neuronal migration defects

By Sossey-Alaoui K.  

Human Molecular Genetics, Vol. 7, Iss. 8, 1998-08 ,pp. : 1327-1332

Oxford University Press

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A Model of Corrective Gene Transfer in X-Linked Ichthyosis

By Freiberg Rachel A.  

Human Molecular Genetics, Vol. 6, Iss. 6, 1997-01 ,pp. : 927-933

Oxford University Press

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Gene expression analysis in a canine model of X-linked Alport syndrome

By Greer Kimberly   Higgins Marnie   Cox Melissa   Ryan Timothy   Berridge Brian   Kashtan Clifford   Lees George   Murphy Keith  

Mammalian Genome, Vol. 17, Iss. 9, 2006-09 ,pp. : 976-990

Springer Publishing Company

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