Found: 15
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Issue Information.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 1, doi. 10.1002/pd.5958
- Publication type:
- Article
Knowledge, attitudes, and practices of healthcare professionals working in prenatal diagnosis toward expanded non‐invasive prenatal testing in China.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 3, doi. 10.1002/pd.6075
- By:
- Publication type:
- Article
Development of standard definitions and grading for Maternal and Fetal Adverse Event Terminology.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 15, doi. 10.1002/pd.6047
- By:
- Publication type:
- Article
Factors impacting surgical decision making between prenatal and postnatal repair for myelomeningocele.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 27, doi. 10.1002/pd.6080
- By:
- Publication type:
- Article
Perinatal outcomes after selective feticide via umbilical cord occlusion in complicated monochorionic pregnancies: A systematic review and meta‐analysis.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 37, doi. 10.1002/pd.6064
- By:
- Publication type:
- Article
Exploring a new paradigm for the fetal anomaly ultrasound scan: Artificial intelligence in real time.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 49, doi. 10.1002/pd.6059
- By:
- Publication type:
- Article
Utility of expanded carrier screening in pregnancies with ultrasound abnormalities.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 60, doi. 10.1002/pd.6069
- By:
- Publication type:
- Article
Pregnancy outcomes of fetuses with congenital heart disease after a prenatal diagnosis with chromosome microarray.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 79, doi. 10.1002/pd.6078
- By:
- Publication type:
- Article
A systematic review of maternal TORCH serology as a screen for suspected fetal infection.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 87, doi. 10.1002/pd.6073
- By:
- Publication type:
- Article
What's out there for parents? A systematic review of online information about prenatal microarray and exome sequencing.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 97, doi. 10.1002/pd.6066
- By:
- Publication type:
- Article
Severe fetal ventriculomegaly: Fetal morbidity and mortality, caesarean delivery rates and obstetrical challenges in a large prospective cohort.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 109, doi. 10.1002/pd.6072
- By:
- Publication type:
- Article
Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 118, doi. 10.1002/pd.6074
- By:
- Publication type:
- Article
Two cases of microvillus inclusion disease caused by MYO5B deficiency with prenatal abnormalities.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 136, doi. 10.1002/pd.6068
- By:
- Publication type:
- Article
S100B in maternal circulation of pregnancies complicated by FGR and brain sparing.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 141, doi. 10.1002/pd.6045
- By:
- Publication type:
- Article
Microvillus inclusion disease with prenatal ultrasound findings and postpartum confirmed.
- Published in:
- 2022
- By:
- Publication type:
- journal article