A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound.
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| Title: | A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound. |
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| Authors: | Corsten-Janssen N; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Bouman K; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Diphoorn JCD; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Scheper AJ; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Kinds R; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., El Mecky J; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.; Clinical Ethics and Law, University of Southampton, Southampton, UK., Breet H; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Verheij JBGM; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Suijkerbuijk R; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Duin LK; Department of Obstetrics, Gynecology and Prenatal Diagnosis, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Manten GTR; Department of Obstetrics and Gynecology, Isala, Zwolle, The Netherlands., van Langen IM; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Sijmons RH; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Sikkema-Raddatz B; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Westers H; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., van Diemen CC; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands. |
| Source: | Prenatal diagnosis [Prenat Diagn] 2020 Sep; Vol. 40 (10), pp. 1300-1309. Date of Electronic Publication: 2020 Jul 20. |
| Publication Type: | Evaluation Study; Journal Article |
| Journal Info: | Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1097-0223 |
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| DOI: | 10.1002/pd.5781 |
