Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis.

van Bon, B W M; Koolen, D A; Borgatti, R; Magee, A; Garcia-Minaur, S; Rooms, L; Reardon, W; Zollino, M; Bonaglia, M C; De Gregori, M; Novara, F; Grasso, R; Ciccone, R; van Duyvenvoorde, H A; Aalbers, A M; Guerrini, R; Fazzi, E; Nillesen, W M; McCullough, S; Kant, S G; Marcelis, C L; Pfundt, R; de Leeuw, N; Smeets, D; Sistermans, E A; Wit, J M; Hamel, B C; Brunner, H G; Kooy, F; Zuffardi, O; de Vries, B B A

van Bon, B W M; Koolen, D A; Borgatti, R; Magee, A; Garcia-Minaur, S; Rooms, L; Reardon, W; Zollino, M; Bonaglia, M C; De Gregori, M; Novara, F; Grasso, R; Ciccone, R; van Duyvenvoorde, H A; Aalbers, A M; Guerrini, R; Fazzi, E; Nillesen, W M; McCullough, S; Kant, S G; Marcelis, C L; Pfundt, R; de Leeuw, N; Smeets, D; Sistermans, E A; Wit, J M; Hamel, B C; Brunner, H G; Kooy, F; Zuffardi, O; de Vries, B B A.

van Bon BW; Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

J Med Genet ; 45(6): 346-54, 2008 Jun.

Article en En | MEDLINE | ID: mdl-18178631

Asunto(s)

Agenesia del Cuerpo Calloso; Deleción Cromosómica; Cromosomas Humanos Par 1/genética; Adolescente; Adulto; Niño; Preescolar; Familia; Femenino; Humanos; Lactante; Masculino; Síndrome

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 1 / Deleción Cromosómica / Agenesia del Cuerpo Calloso Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Año: 2008 Tipo del documento: Article

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