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A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHD.
Bertelsen, Birgitte; Melchior, Linea; Jensen, Lars Riff; Groth, Camilla; Nazaryan, Lusine; Debes, Nanette Mol; Skov, Liselotte; Xie, Gangcai; Sun, Wei; Brøndum-Nielsen, Karen; Kuss, Andreas Walter; Chen, Wei; Tümer, Zeynep.
Afiliación
  • Bertelsen B; Department of Clinical Genetics, Applied Human Molecular Genetics, Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Glostrup, Denmark.
  • Melchior L; Department of Clinical Genetics, Applied Human Molecular Genetics, Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Glostrup, Denmark.
  • Jensen LR; Department of Human Genetics, University Medicine Greifswald and Interfaculty Institute of Genetics and Functional Genomics, University of Greifswald, Greifswald, Germany.
  • Groth C; Tourette Clinic, Department of Pediatrics, Copenhagen University Hospital, Herlev Hospital, Herlev, Denmark.
  • Nazaryan L; Department of Clinical Genetics, Applied Human Molecular Genetics, Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Glostrup, Denmark.
  • Debes NM; Tourette Clinic, Department of Pediatrics, Copenhagen University Hospital, Herlev Hospital, Herlev, Denmark.
  • Skov L; Tourette Clinic, Department of Pediatrics, Copenhagen University Hospital, Herlev Hospital, Herlev, Denmark.
  • Xie G; Max Delbrück Center for Molecular Medicine, Berlin Institute for Medical Systems Biology, Berlin, Germany.
  • Sun W; Max Delbrück Center for Molecular Medicine, Berlin Institute for Medical Systems Biology, Berlin, Germany.
  • Brøndum-Nielsen K; Department of Clinical Genetics, Applied Human Molecular Genetics, Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Glostrup, Denmark.
  • Kuss AW; Department of Human Genetics, University Medicine Greifswald and Interfaculty Institute of Genetics and Functional Genomics, University of Greifswald, Greifswald, Germany.
  • Chen W; Max Delbrück Center for Molecular Medicine, Berlin Institute for Medical Systems Biology, Berlin, Germany.
  • Tümer Z; Department of Clinical Genetics, Applied Human Molecular Genetics, Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Glostrup, Denmark. Electronic address: zeynep.tumer@regionh.dk.
Psychiatry Res ; 225(3): 268-75, 2015 Feb 28.
Article en En | MEDLINE | ID: mdl-25595337
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno por Déficit de Atención con Hiperactividad / Translocación Genética / Cromosomas Humanos Par 3 / Cromosomas Humanos Par 9 / Glicoproteínas / Síndrome de Tourette / Proteínas de la Matriz Extracelular / Trastorno Obsesivo Compulsivo Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Psychiatry Res Año: 2015 Tipo del documento: Article País de afiliación: Dinamarca Pais de publicación: Irlanda
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno por Déficit de Atención con Hiperactividad / Translocación Genética / Cromosomas Humanos Par 3 / Cromosomas Humanos Par 9 / Glicoproteínas / Síndrome de Tourette / Proteínas de la Matriz Extracelular / Trastorno Obsesivo Compulsivo Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Psychiatry Res Año: 2015 Tipo del documento: Article País de afiliación: Dinamarca Pais de publicación: Irlanda