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Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGH.
Caselli, R; Speciale, C; Pescucci, C; Uliana, V; Sampieri, K; Bruttini, M; Longo, I; De Francesco, S; Pramparo, T; Zuffardi, O; Frezzotti, R; Acquaviva, A; Hadjistilianou, T; Renieri, A; Mari, F.
Afiliación
  • Caselli R; Medical Genetics, Department of Molecular Biology, University of Siena, Policlinico Le Scotte, V.le Bracci 2, 53100, Siena, Italy.
  • Speciale C; Medical Genetics, Department of Molecular Biology, University of Siena, Policlinico Le Scotte, V.le Bracci 2, 53100, Siena, Italy.
  • Pescucci C; Medical Genetics, Department of Molecular Biology, University of Siena, Policlinico Le Scotte, V.le Bracci 2, 53100, Siena, Italy.
  • Uliana V; Medical Genetics, Department of Molecular Biology, University of Siena, Policlinico Le Scotte, V.le Bracci 2, 53100, Siena, Italy.
  • Sampieri K; Medical Genetics, Department of Molecular Biology, University of Siena, Policlinico Le Scotte, V.le Bracci 2, 53100, Siena, Italy.
  • Bruttini M; Medical Genetics, Department of Molecular Biology, University of Siena, Policlinico Le Scotte, V.le Bracci 2, 53100, Siena, Italy.
  • Longo I; Medical Genetics, Department of Molecular Biology, University of Siena, Policlinico Le Scotte, V.le Bracci 2, 53100, Siena, Italy.
  • De Francesco S; Department of Ophthalmology, Retinoblastoma Referral Center, Siena, Italy.
  • Pramparo T; Biologia Generale e Genetica Medica, University of Pavia, Pavia, Italy.
  • Zuffardi O; Biologia Generale e Genetica Medica, University of Pavia, Pavia, Italy.
  • Frezzotti R; Department of Ophthalmology, University of Siena, Siena, Italy.
  • Acquaviva A; Department of Pediatrics, University of Siena, Siena, Italy.
  • Hadjistilianou T; Department of Ophthalmology, Retinoblastoma Referral Center, Siena, Italy.
  • Renieri A; Medical Genetics, Department of Molecular Biology, University of Siena, Policlinico Le Scotte, V.le Bracci 2, 53100, Siena, Italy. renieri@unisi.it.
  • Mari F; Medical Genetics, Department of Molecular Biology, University of Siena, Policlinico Le Scotte, V.le Bracci 2, 53100, Siena, Italy.
J Hum Genet ; 52(6): 535-542, 2007.
Article en En | MEDLINE | ID: mdl-17502991
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retinoblastoma / Anomalías Múltiples / Deleción Cromosómica / Neoplasias de la Retina / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2007 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retinoblastoma / Anomalías Múltiples / Deleción Cromosómica / Neoplasias de la Retina / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2007 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido