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Prenatal Diagnosis of an Uncommon 48,XX,+18+21 Karyotype in a Fetus With Malformations Typical of Both Trisomies.
Fiorio, Patrizia; Donarini, Gloria; Fulcheri, Ezio; Meccariello, Gabriella; Tassano, Elisa; Amico, Giulia; Paladini, Dario.
  • Fiorio P; Human Genetics Unit, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.
  • Donarini G; Fetal Medicine and Surgery Unit, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.
  • Fulcheri E; Fetal and Perinatal Pathology Unit, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.
  • Meccariello G; Division of Anatomic Pathology, Department of Surgical and Diagnostic Sciences, University of Genoa, Genoa, Italy.
  • Tassano E; Fetal Medicine and Surgery Unit, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.
  • Amico G; Human Genetics Unit, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.
  • Paladini D; Genetics and Genomics of Rare Diseases Unit, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.
J Ultrasound Med ; 39(11): 2277-2279, 2020 Nov.
Article en En | MEDLINE | ID: mdl-32412111
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Trisomía Límite: Female / Humans / Pregnancy Idioma: En Año: 2020 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Trisomía Límite: Female / Humans / Pregnancy Idioma: En Año: 2020 Tipo del documento: Article