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Fetal aneuploidy diagnosed at celocentesis for early prenatal diagnosis of congenital hemoglobinopathies.
Giambona, Antonino; Leto, Filippo; Passarello, Cristina; Vinciguerra, Margherita; Cigna, Valentina; Schillaci, Giovanna; Picciotto, Francesco; Lauricella, Salvatrice; Nicolaides, Kypros H; Makrydimas, George; Damiani, Gianfranca; Maggio, Aurelio.
Afiliação
  • Giambona A; Unit of Hematology for Rare Diseases of the Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Hospital Villa Sofia Cervello, Palermo, Italy.
  • Leto F; Unit of Hematology for Rare Diseases of the Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Hospital Villa Sofia Cervello, Palermo, Italy.
  • Passarello C; Unit of Hematology for Rare Diseases of the Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Hospital Villa Sofia Cervello, Palermo, Italy.
  • Vinciguerra M; Unit of Hematology for Rare Diseases of the Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Hospital Villa Sofia Cervello, Palermo, Italy.
  • Cigna V; Unit of Prenatal Diagnosis, Hospital Villa Sofia Cervello, Palermo, Italy.
  • Schillaci G; Unit of Prenatal Diagnosis, Hospital Villa Sofia Cervello, Palermo, Italy.
  • Picciotto F; Unit of Prenatal Diagnosis, Hospital Villa Sofia Cervello, Palermo, Italy.
  • Lauricella S; Laboratory of Cytogenetics, Hospital Villa Sofia Cervello, Palermo, Italy.
  • Nicolaides KH; Harris Birthright Research Center for Fetal Medicine, King's College, London, UK.
  • Makrydimas G; Obstetrics and Gynecology, Ioannina University Hospital, Ioannina, Greece.
  • Damiani G; Unit of Prenatal Diagnosis, Hospital Villa Sofia Cervello, Palermo, Italy.
  • Maggio A; Unit of Hematology for Rare Diseases of the Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Hospital Villa Sofia Cervello, Palermo, Italy.
Acta Obstet Gynecol Scand ; 97(3): 312-321, 2018 Mar.
Article em En | MEDLINE | ID: mdl-29292496
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Síndrome de Down / Triploidia / Síndrome da Trissomia do Cromossomo 13 / Hemoglobinopatias Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Acta Obstet Gynecol Scand Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Síndrome de Down / Triploidia / Síndrome da Trissomia do Cromossomo 13 / Hemoglobinopatias Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Acta Obstet Gynecol Scand Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália País de publicação: Estados Unidos