Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region

By Froyen Guy   Bauters Marijke   Boyle Jackie   Esch Hilde   Govaerts Karen   Bokhoven Hans   Ropers Hans-Hilger   Moraine Claude   Chelly Jamel   Fryns Jean-Pierre   Marynen Peter   Gecz Jozef   Turner Gillian  

Human Genetics, Vol. 121, Iss. 5, 2007-06 ,pp. : 539-547

Springer Publishing Company

Access to resources Recommend Favorite

CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior

By Hollanders K.  

Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1463-1474

Oxford University Press

Access to resources Recommend Favorite

Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor

By Ropers H-H.  

Human Molecular Genetics, Vol. 7, Iss. 8, 1998-08 ,pp. : 1311-1315

Oxford University Press

Access to resources Recommend Favorite

Localization of a Non-Specific X-linked Mental Retardation Gene, MRX23, to Xq23–q24

By Gregg Ronald G.   Palmer Christina   Kirkpatrick Susan   Simantel Amy  

Human Molecular Genetics, Vol. 5, Iss. 3, 1996-01 ,pp. : 411-414

Oxford University Press

Access to resources Recommend Favorite

Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation

By Ylisaukko-oja Tero   Rehnström Karola   Vanhala Raija   Tengström Carola   Lähdetie Jaana   Järvelä Irma  

Human Genetics, Vol. 114, Iss. 2, 2004-01 ,pp. : 211-213

Springer Publishing Company

Access to resources Recommend Favorite