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HBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB Gene.
Vinciguerra, Margherita; Cannata, Monica; Cassarà, Filippo; Passarello, Cristina; Leto, Filippo; Calvaruso, Giuseppina; Renda, Disma; Maggio, Aurelio; Giambona, Antonino.
Afiliação
  • Vinciguerra M; a Department of Hematology for Rare Diseases of Blood and Blood-Forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases , Villa Sofia-Cervello Hospital , Palermo , Italy.
  • Cannata M; a Department of Hematology for Rare Diseases of Blood and Blood-Forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases , Villa Sofia-Cervello Hospital , Palermo , Italy.
  • Cassarà F; a Department of Hematology for Rare Diseases of Blood and Blood-Forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases , Villa Sofia-Cervello Hospital , Palermo , Italy.
  • Passarello C; a Department of Hematology for Rare Diseases of Blood and Blood-Forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases , Villa Sofia-Cervello Hospital , Palermo , Italy.
  • Leto F; a Department of Hematology for Rare Diseases of Blood and Blood-Forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases , Villa Sofia-Cervello Hospital , Palermo , Italy.
  • Calvaruso G; a Department of Hematology for Rare Diseases of Blood and Blood-Forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases , Villa Sofia-Cervello Hospital , Palermo , Italy.
  • Renda D; a Department of Hematology for Rare Diseases of Blood and Blood-Forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases , Villa Sofia-Cervello Hospital , Palermo , Italy.
  • Maggio A; a Department of Hematology for Rare Diseases of Blood and Blood-Forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases , Villa Sofia-Cervello Hospital , Palermo , Italy.
  • Giambona A; a Department of Hematology for Rare Diseases of Blood and Blood-Forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases , Villa Sofia-Cervello Hospital , Palermo , Italy.
Hemoglobin ; 41(4-6): 234-238, 2017.
Article em En | MEDLINE | ID: mdl-29171316
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hemoglobinas / Íntrons / Família Multigênica / Mutação Puntual / Polimorfismo de Nucleotídeo Único Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged / Pregnancy País/Região como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hemoglobinas / Íntrons / Família Multigênica / Mutação Puntual / Polimorfismo de Nucleotídeo Único Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged / Pregnancy País/Região como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article