Found: 17
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- Published in:
- Prenatal Diagnosis, 2019, v. 39, n. 11, p. i, doi. 10.1002/pd.5585
- By:
- Publication type:
- Article
Issue Information.
- Published in:
- Prenatal Diagnosis, 2019, v. 39, n. 11, p. 945, doi. 10.1002/pd.5313
- Publication type:
- Article
Blood-based biomarkers in the maternal circulation associated with fetal growth restriction.
- Published in:
- 2019
- By:
- Publication type:
- journal article
The failure of non-invasive prenatal testing due to maternal dermatomyositis.
- Published in:
- 2019
- By:
- Publication type:
- journal article
The association between severe fetal congenital heart defects and placental vascular malperfusion lesions.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Risk of congenital heart diseases associated with NAT2 genetic polymorphisms and maternal polycyclic aromatic hydrocarbons exposure.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Uterine artery and umbilical vein blood flow are unaffected by moderate habitual physical activity during pregnancy.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non-homologous Robertsonian translocation. Should we still perform prenatal diagnosis?
- Published in:
- 2019
- By:
- Publication type:
- journal article
Prenatal diagnosis of methylmalonic aciduria from amniotic fluid using genetic and biochemical approaches.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Clinical and genetic description of patients with prenatally identified cardiac tumors.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Determining gestational age using genome methylation profile: A novel approach for fetal medicine.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Clinical validation of a novel automated cell-free DNA screening assay for trisomies 21, 13, and 18 in maternal plasma.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Placental studies elucidate discrepancies between NIPT showing a structural chromosome aberration and a differently abnormal fetal karyotype.
- Published in:
- 2019
- By:
- Publication type:
- journal article
SOX3 duplication: A genetic cause to investigate in fetuses with neural tube defects.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Isolated spina bifida aperta: prenatal ventriculomegaly as an ultrasound prognostic marker.
- Published in:
- 2019
- By:
- Publication type:
- letter
Comment on "Expanded carrier screening for autosomal recessive conditions in health care: Arguments for a couple-based approach and examination of couples' views".
- Published in:
- 2019
- By:
- Publication type:
- letter
Is it feasible to select fetuses for prenatal WES based on the prenatal phenotype?
- Published in:
- 2019
- By:
- Publication type:
- letter