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Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome.
Jiraanont, P; Hagerman, R J; Neri, G; Zollino, M; Murdolo, M; Tassone, F.
Afiliación
  • Jiraanont P; Department of Biochemistry and Molecular Medicine, University of California Davis, Davis, CA, USA; Research Center for Neuroscience, Institute of Molecular Biosciences, Mahidol University, Nakornpathom, Thailand.
  • Hagerman RJ; Department of Pediatrics, University of California Davis, Davis, CA, USA; MIND Institute, School of Medicine, University of California Davis, Davis, CA, USA.
  • Neri G; Institute of Medical Genetics, Catholic University of the Sacred Heart-Agostino Gemelli University Hospital, Rome, Italy.
  • Zollino M; Institute of Medical Genetics, Catholic University of the Sacred Heart-Agostino Gemelli University Hospital, Rome, Italy.
  • Murdolo M; Institute of Medical Genetics, Catholic University of the Sacred Heart-Agostino Gemelli University Hospital, Rome, Italy.
  • Tassone F; Department of Biochemistry and Molecular Medicine, University of California Davis, Davis, CA, USA; MIND Institute, School of Medicine, University of California Davis, Davis, CA, USA. Electronic address: ftassone@ucdavis.edu.
Eur J Med Genet ; 59(9): 459-62, 2016 Sep.
Article en En | MEDLINE | ID: mdl-27546052
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Eliminación de Gen / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil / Mosaicismo Tipo de estudio: Diagnostic_studies Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Eliminación de Gen / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil / Mosaicismo Tipo de estudio: Diagnostic_studies Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article