Prenatal diagnosis of non-immune hydrops fetalis: whole-exome sequencing or whole-genome sequencing?
- PMID: 36183347
- DOI: 10.1002/uog.26063
Prenatal diagnosis of non-immune hydrops fetalis: whole-exome sequencing or whole-genome sequencing?
Comment in
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Reply.Ultrasound Obstet Gynecol. 2022 Oct;60(4):586. doi: 10.1002/uog.26064. Ultrasound Obstet Gynecol. 2022. PMID: 36183348 No abstract available.
Comment on
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Diagnostic yield using whole-genome sequencing and in-silico panel of 281 genes associated with non-immune hydrops fetalis in clinical setting.Ultrasound Obstet Gynecol. 2022 Oct;60(4):487-493. doi: 10.1002/uog.24911. Epub 2022 Aug 30. Ultrasound Obstet Gynecol. 2022. PMID: 35397126 Free PMC article.
References
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- Steurer MA, Peyvandi S, Baer RJ, MacKenzie T, Li BC, Norton ME, Jelliffe-Pawlowski LL, Moon-Grady AJ. Epidemiology of live born infants with nonimmune hydrops fetalis - Insights from a population-based dataset. J Pediatr 2017; 187: 182-188.
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- Westenius E, Sahlin E, Conner P, Lindstrand A, Iwarsson E. Diagnostic yield using whole-genome sequencing and in-silico gene panel of 281 genes associated with non-immune hydrops fetalis in clinical setting. Ultrasound Obstet Gynecol 2022; 60: 487-493.
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- Lappalainen T, Scott AJ, Brandt M, Hall IM. Genomic analysis in the age of human genome sequencing. Cell 2019; 177: 70-84.
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- Dong X, Liu B, Yang L, Wang H, Wu B, Liu R, Chen H, Chen X, Yu S, Chen B, Wang S, Xu X, Zhou W, Lu Y. Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort. J Med Genet 2020; 57: 558-566.
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