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MDS/AML del(11)(q14) Share Common Morphological Features Despite Different Chromosomal Breakpoints.
Dambruoso, Irene; Invernizzi, Rosangela; Boni, Marina; Zappatore, Rita; Giardini, Ilaria; Cavigliano, Maria Paola; Rocca, Barbara; Calvello, Celeste; Bastia, Raffaella; Caresana, Marilena; Pasi, Francesca; Nano, Rosanna; Bernasconi, Paolo.
Afiliação
  • Dambruoso I; Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy i.dambruoso@smatteo.pv.it.
  • Invernizzi R; Division of Internal Medicine, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Boni M; Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Zappatore R; Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Giardini I; Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Cavigliano MP; Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Rocca B; Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Calvello C; Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Bastia R; Division of Internal Medicine, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Caresana M; Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Pasi F; Division of Radiotherapy, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Nano R; Laboratory of Neuro Radio Experimental Biology, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, Pavia, Italy.
  • Bernasconi P; Laboratory of Neuro Radio Experimental Biology, Department of Biology and Biotechnology "L. Spallanzani", University of Pavia, Pavia, Italy.
Anticancer Res ; 37(2): 645-649, 2017 02.
Article em En | MEDLINE | ID: mdl-28179312
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Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Cromossomos Humanos Par 11 / Leucemia Mieloide / Deleção Cromossômica / Pontos de Quebra do Cromossomo Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Buscar no Google
Imprimir
XML
PubMed Links

Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Cromossomos Humanos Par 11 / Leucemia Mieloide / Deleção Cromossômica / Pontos de Quebra do Cromossomo Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article