Publication | Open Access
Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis
183
Citations
28
References
2020
Year
In this large case series of 127 fetuses with unexplained NIHF, we identified a diagnostic genetic variant in approximately one third of the cases. (Funded by the UCSF Center for Maternal-Fetal Precision Medicine and others; ClinicalTrials.gov number, NCT03412760.).
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