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Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Petrovski, Slavé; Aggarwal, Vimla; Giordano, Jessica L; Stosic, Melissa; Wou, Karen; Bier, Louise; Spiegel, Erica; Brennan, Kelly; Stong, Nicholas; Jobanputra, Vaidehi; Ren, Zhong; Zhu, Xiaolin; Mebane, Caroline; Nahum, Odelia; Wang, Quanli; Kamalakaran, Sitharthan; Malone, Colin; Anyane-Yeboa, Kwame; Miller, Russell; Levy, Brynn; Goldstein, David B; Wapner, Ronald J.
Afiliación
  • Petrovski S; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA; AstraZeneca Centre for Genomics Research, Precision Medicine and Genomics, IMED Biotech Unit, AstraZeneca, Cambridge, UK.
  • Aggarwal V; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA; Laboratory of Personalized Genomic Medicine, Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.
  • Giordano JL; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA; Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Columbia University Medical Center, New York, NY, USA.
  • Stosic M; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA; Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Columbia University Medical Center, New York, NY, USA.
  • Wou K; Division of Clinical Genetics, Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
  • Bier L; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.
  • Spiegel E; Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Columbia University Medical Center, New York, NY, USA.
  • Brennan K; Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Columbia University Medical Center, New York, NY, USA.
  • Stong N; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.
  • Jobanputra V; Laboratory of Personalized Genomic Medicine, Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.
  • Ren Z; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.
  • Zhu X; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.
  • Mebane C; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.
  • Nahum O; Laboratory of Personalized Genomic Medicine, Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.
  • Wang Q; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.
  • Kamalakaran S; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.
  • Malone C; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.
  • Anyane-Yeboa K; Division of Clinical Genetics, Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
  • Miller R; Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Columbia University Medical Center, New York, NY, USA.
  • Levy B; Laboratory of Personalized Genomic Medicine, Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.
  • Goldstein DB; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA; Department of Genetics and Development, Columbia University Medical Center, New York, NY, USA.
  • Wapner RJ; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA; Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Columbia University Medical Center, New York, NY, USA. Electronic address: rw2191@cumc.columbia.edu.
Lancet ; 393(10173): 758-767, 2019 02 23.
Article en En | MEDLINE | ID: mdl-30712878
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Desarrollo Fetal / Variaciones en el Número de Copia de ADN / Feto / Cariotipo Anormal / Secuenciación del Exoma / Aneuploidia Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Pregnancy Idioma: En Revista: Lancet Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
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XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Desarrollo Fetal / Variaciones en el Número de Copia de ADN / Feto / Cariotipo Anormal / Secuenciación del Exoma / Aneuploidia Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Pregnancy Idioma: En Revista: Lancet Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido