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13q Deletion Syndrome Involving RB1: Characterization of a New Minimal Critical Region for Psychomotor Delay.
Privitera, Flavia; Calonaci, Arianna; Doddato, Gabriella; Papa, Filomena Tiziana; Baldassarri, Margherita; Pinto, Anna Maria; Mari, Francesca; Longo, Ilaria; Caini, Mauro; Galimberti, Daniela; Hadjistilianou, Theodora; De Francesco, Sonia; Renieri, Alessandra; Ariani, Francesca.
Afiliación
  • Privitera F; Medical Genetics, University of Siena, 53100 Siena, Italy.
  • Calonaci A; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, 53100 Siena, Italy.
  • Doddato G; Unit of Pediatrics, Department of Maternal, Newborn and Child Health, Azienda Ospedaliera Universitaria Senese, Policlinico 'Santa Maria alle Scotte', 53100 Siena, Italy.
  • Papa FT; Medical Genetics, University of Siena, 53100 Siena, Italy.
  • Baldassarri M; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, 53100 Siena, Italy.
  • Pinto AM; Medical Genetics, University of Siena, 53100 Siena, Italy.
  • Mari F; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, 53100 Siena, Italy.
  • Longo I; Medical Genetics, University of Siena, 53100 Siena, Italy.
  • Caini M; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, 53100 Siena, Italy.
  • Galimberti D; Genetica Medica, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy.
  • Hadjistilianou T; Medical Genetics, University of Siena, 53100 Siena, Italy.
  • De Francesco S; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, 53100 Siena, Italy.
  • Renieri A; Genetica Medica, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy.
  • Ariani F; Genetica Medica, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy.
Genes (Basel) ; 12(9)2021 08 26.
Article en En | MEDLINE | ID: mdl-34573300
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Deleción Cromosómica / Trastornos de los Cromosomas Idioma: En Revista: Genes (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Italia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Deleción Cromosómica / Trastornos de los Cromosomas Idioma: En Revista: Genes (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Italia