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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doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

By Ricci S.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1063-1070

Oxford University Press

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Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophy

By Unterrainer Gertraud   Molzer Brunhilde   Forss-Petter Sonja   Berger Johannes  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2609-2616

Oxford University Press

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Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3

By Cheetham M.E.  

Human Molecular Genetics, Vol. 11, Iss. 24, 2002-09 ,pp. : 3065-3074

Oxford University Press

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MECP2 is highly mutated in X-linked mental retardation

By Souville I.  

Human Molecular Genetics, Vol. 10, Iss. 9, 2001-04 ,pp. : 941-946

Oxford University Press

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