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Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: Disappearance of cytogenetic abnormalities.
Vyrides, Niki; Douka, Vassiliki; Gavriilaki, Eleni; Papaioannou, Georgios; Athanasiadou, Anastasia; Neofytou, Sofia; Vyrides, Yiannis; Lalayanni, Chrysavgi; Anagnostopoulos, Achilles; Kokoris, Styliani I.
Afiliação
  • Vyrides N; Haematology Department, Vyrides Clinic, Nicosia, Cyprus; University of Nicosia Medical School, Nicosia, Cyprus. Electronic address: vyrides.n@unic.ac.cy.
  • Douka V; Hematology Department-BMT Unit, G. Papanicolaou Hospital, Thessaloniki; Greece.
  • Gavriilaki E; Hematology Department-BMT Unit, G. Papanicolaou Hospital, Thessaloniki; Greece.
  • Papaioannou G; Hematology Department-BMT Unit, G. Papanicolaou Hospital, Thessaloniki; Greece.
  • Athanasiadou A; Hematology Department-BMT Unit, G. Papanicolaou Hospital, Thessaloniki; Greece.
  • Neofytou S; Cytogenetic Department, Archbishop Makarios III Hospital - Nicosia, Cyprus.
  • Vyrides Y; Great Western Hospitals NHS Foundation Trust, Swindon, United Kingdom.
  • Lalayanni C; Hematology Department-BMT Unit, G. Papanicolaou Hospital, Thessaloniki; Greece.
  • Anagnostopoulos A; Hematology Department-BMT Unit, G. Papanicolaou Hospital, Thessaloniki; Greece.
  • Kokoris SI; Laboratory of Hematology and Hospital Blood Transfusion Department, University General Hospital "Attikon", National and Kapodistrian University of Athens, Medical School, Greece.
Cancer Genet ; 250-251: 1-5, 2021 01.
Article em En | MEDLINE | ID: mdl-33188967
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Aberrações Cromossômicas / Hemoglobinúria Paroxística Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Aberrações Cromossômicas / Hemoglobinúria Paroxística Idioma: En Ano de publicação: 2021 Tipo de documento: Article