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Performance of a targeted cell-free DNA prenatal test for 22q11.2 deletion in a large clinical cohort.
Bevilacqua, E; Jani, J C; Chaoui, R; Suk, E-K A; Palma-Dias, R; Ko, T-M; Warsof, S; Stokowski, R; Jones, K J; Grati, F R; Schmid, M.
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  • Bevilacqua E; Department of Obstetrics and Gynecology, University Hospital Brugmann, Université Libre de Bruxelles, Brussels, Belgium.
  • Jani JC; Department of Obstetrics and Gynecology, University Hospital Brugmann, Université Libre de Bruxelles, Brussels, Belgium.
  • Chaoui R; Prenatal Diagnosis and Human Genetics, Berlin, Germany.
  • Suk EA; Prenatal Diagnosis and Human Genetics, Berlin, Germany.
  • Palma-Dias R; The Royal Women's Hospital, University of Melbourne, Parkville, VIC, Australia.
  • Ko TM; Genephile Bioscience Laboratory, Ko's Obstetrics & Gynecology Clinic, Taipei City, Taiwan.
  • Warsof S; Eastern Virginia Medical School, Norfolk, VA, USA.
  • Stokowski R; Roche Sequencing Solutions, Inc., San Jose, CA, USA.
  • Jones KJ; Roche Sequencing Solutions, Inc., San Jose, CA, USA.
  • Grati FR; TOMA Advanced Biomedical Assays S.p.A, Impact Lab., Busto Arsizio, Italy.
  • Schmid M; Roche Sequencing Solutions, Inc., San Jose, CA, USA.
Ultrasound Obstet Gynecol ; 58(4): 597-602, 2021 Oct.
Article en En | MEDLINE | ID: mdl-34090308
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de DiGeorge / Pruebas de Detección del Suero Materno / Ácidos Nucleicos Libres de Células Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Año: 2021 Tipo del documento: Article
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de DiGeorge / Pruebas de Detección del Suero Materno / Ácidos Nucleicos Libres de Células Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Año: 2021 Tipo del documento: Article