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2. A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies. (20th May 2022)

6. Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies. (1st February 2022)

7. Diagnostic yield of whole exome data in fetuses aborted for conotruncal malformations. (23rd April 2022)

9. Exploring the diagnostic utility of genome sequencing for fetal congenital heart defects. (27th April 2022)

10. Factors that impact on women's decision‐making around prenatal genomic tests: An international discrete choice survey. (30th April 2022)