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- PMID: 38695203
- DOI: 10.1002/uog.27651
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References
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- Westenius E, Conner P, Pettersson M, et al. Whole‐genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting. Ultrasound Obstet Gynecol. 2024;63:658‐663.
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- Qi Q, Jiang Y, Zhou X, et al. Whole genome sequencing analysis in fetal structural anomalies: novel phenotype–genotype discoveries. Ultrasound Obstet Gynecol. 2024;63:664‐671.
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