The utility of exome sequencing for fetal pleural effusions.

Jelin, Angie C; Sobreira, Nara; Wohler, Elizabeth; Solomon, Benjamin; Sparks, Teresa; Sagaser, Katelynn G; Forster, Katherine R; Miller, Jena; Witmer, P Dane; Hamosh, Ada; Valle, David; Blakemore, Karin

Jelin, Angie C; Sobreira, Nara; Wohler, Elizabeth; Solomon, Benjamin; Sparks, Teresa; Sagaser, Katelynn G; Forster, Katherine R; Miller, Jena; Witmer, P Dane; Hamosh, Ada; Valle, David; Blakemore, Karin.

Afiliación

Jelin AC; Department of Gynecology and Obstetrics, Division of Maternal Fetal Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Sobreira N; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, MD, USA.
Wohler E; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, MD, USA.
Solomon B; Baylor-Hopkins Center for Mendelian Genomics, Baltimore, MD, USA.
Sparks T; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, MD, USA.
Sagaser KG; Baylor-Hopkins Center for Mendelian Genomics, Baltimore, MD, USA.
Forster KR; GeneDx, Bethesda, MD, USA.
Miller J; Department of Obstetrics, Gynecology & Reproductive Sciences, Division of Maternal Fetal Medicine, University of California, San Francisco, CA, USA.
Witmer PD; Department of Gynecology and Obstetrics, Division of Maternal Fetal Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Hamosh A; Department of Gynecology and Obstetrics, Center for Fetal Therapy, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Valle D; Department of Gynecology and Obstetrics, Center for Fetal Therapy, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Blakemore K; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, MD, USA.

Prenat Diagn ; 40(5): 590-595, 2020 04.

Article en En | MEDLINE | ID: mdl-31994743

Asunto(s)

Secuenciación del Exoma; Enfermedades Fetales/genética; Derrame Pleural/genética; Actinina/genética; Moléculas de Adhesión Celular/genética; Estudios de Cohortes; Proteínas de la Matriz Extracelular/genética; Pestañas/anomalías; Femenino; Enfermedades Fetales/diagnóstico por imagen; Factores de Transcripción Forkhead/genética; Humanos; Linfedema/diagnóstico; Linfedema/genética; Derrame Pleural/diagnóstico por imagen; Embarazo; Estudios Prospectivos; Receptor EphB4/genética; Canal Liberador de Calcio Receptor de Rianodina/genética

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Derrame Pleural / Enfermedades Fetales / Secuenciación del Exoma Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Prenat Diagn Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

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