Your browser doesn't support javascript.
loading
Prenatal diagnosis study using array comparative genomic hybridization for genotype-phenotype correlation in 772 fetuses.
Costa, Beatriz C; Grangeia, Ana; Galvão, Joana; Vaz, Diane; Melo, Mónica; Carraca, Teresa; Ramalho, Carla; Dória, Sofia.
Afiliación
  • Costa BC; Department of Pathology, Genetics Service, Faculty of Medicine, University of Porto, Portugal.
  • Grangeia A; Department of Pathology, Genetics Service, Faculty of Medicine, University of Porto, Portugal; Medical Genetics Service, Centro Hospitalar Universitário de São João, Porto, Portugal; I3S-Instituto de Investigação e Inovação em Saúde, University of Porto, Porto, Portugal.
  • Galvão J; Department of Obstetrics and Gynecology, Centro Hospitalar Vila Nova Gaia/Espinho (CHVNG), Vila Nova de Gaia, Portugal.
  • Vaz D; Department of Pathology, Genetics Service, Faculty of Medicine, University of Porto, Portugal.
  • Melo M; Department of Obstetrics and Gynecology, Centro Hospitalar Vila Nova Gaia/Espinho (CHVNG), Vila Nova de Gaia, Portugal.
  • Carraca T; Department of Obstetrics and Gynecology, Hospital São João, Porto, Portugal.
  • Ramalho C; I3S-Instituto de Investigação e Inovação em Saúde, University of Porto, Porto, Portugal; Department of Obstetrics and Gynecology, Hospital São João, Porto, Portugal; Obstetrics and Gynecology Service, Faculty of Medicine, Porto, Portugal.
  • Dória S; Department of Pathology, Genetics Service, Faculty of Medicine, University of Porto, Portugal; I3S-Instituto de Investigação e Inovação em Saúde, University of Porto, Porto, Portugal. Electronic address: sdoria@med.up.pt.
Ann Diagn Pathol ; 61: 152059, 2022 Dec.
Article en En | MEDLINE | ID: mdl-36343605
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Aberraciones Cromosómicas / Variaciones en el Número de Copia de ADN Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Ann Diagn Pathol Asunto de la revista: PATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Portugal
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Aberraciones Cromosómicas / Variaciones en el Número de Copia de ADN Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Ann Diagn Pathol Asunto de la revista: PATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Portugal