Your browser doesn't support javascript.
loading
The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing.
Swanson, Kate; Norton, Mary E; Lianoglou, Billie R; Jelin, Angie C; Hodoglugil, Ugur; Van Ziffle, Jessica; Devine, Patrick; Sparks, Teresa N.
  • Swanson K; Department of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal-Fetal Medicine, University of California, San Francisco, California, USA.
  • Norton ME; Department of Pediatrics, Division of Medical Genetics, University of California, San Francisco, California, USA.
  • Lianoglou BR; Department of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal-Fetal Medicine, University of California, San Francisco, California, USA.
  • Jelin AC; Department of Pediatrics, Division of Medical Genetics, University of California, San Francisco, California, USA.
  • Hodoglugil U; Fetal Treatment Center, University of California, San Francisco, California, USA.
  • Van Ziffle J; Institute for Human Genetics, University of California, San Francisco, California, USA.
  • Devine P; Fetal Treatment Center, University of California, San Francisco, California, USA.
  • Sparks TN; Department of Gynecology and Obstetrics, Johns Hopkins Hospital, Baltimore, Maryland, USA.
Prenat Diagn ; 42(10): 1288-1294, 2022 09.
Article en En | MEDLINE | ID: mdl-35723972
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Feto / Exoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Pregnancy Idioma: En Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Feto / Exoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Pregnancy Idioma: En Año: 2022 Tipo del documento: Article