Found: 16
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- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 261, doi. 10.1002/pd.6371
- Publication type:
- Article
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies.
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- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 263, doi. 10.1002/pd.6507
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- Publication type:
- Article
Women's attitudes towards disclosure of genetic information in pregnancy with varying levels of penetrance.
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- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 270, doi. 10.1002/pd.6518
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- Publication type:
- Article
Has the introduction of increased genetic prenatal testing affected rates of termination of pregnancy due to fetal abnormality?
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- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 280, doi. 10.1002/pd.6526
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- Publication type:
- Article
The role of confined placental mosaicism in fetal growth restriction: A retrospective cohort study.
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- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 289, doi. 10.1002/pd.6533
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- Publication type:
- Article
Knowledge gaps and confidence in counseling about aneuploidy screening and testing: A survey of prenatal care clinicians.
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- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 297, doi. 10.1002/pd.6524
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- Publication type:
- Article
Noninvasive single‐cell‐based prenatal genetic testing: A proof of concept clinical study.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 304, doi. 10.1002/pd.6529
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- Publication type:
- Article
Preterm membranes are mechanically more resistant than term membranes.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 317, doi. 10.1002/pd.6511
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- Publication type:
- Article
Predictors of fetal death, neonatal survival and neurological outcomes in severe twin‐twin transfusion syndrome treated by laser ablation of placental vessels.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 325, doi. 10.1002/pd.6523
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- Publication type:
- Article
Ethical reflections on organizing the first human trial of artificial womb technologies.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 336, doi. 10.1002/pd.6521
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- Publication type:
- Article
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease.
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- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 343, doi. 10.1002/pd.6527
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- Article
Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not?
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- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 352, doi. 10.1002/pd.6519
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- Publication type:
- Article
A de novo pathogenic variant in DHX30 gene in a fetus with isolated dysgenesis of the corpus callosum.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 357, doi. 10.1002/pd.6536
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- Publication type:
- Article
Prenatal characterization of novel neurosonographic findings in a fetus with SOTOS syndrome.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 360, doi. 10.1002/pd.6504
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- Publication type:
- Article
Diffuse interstitial lung disease in a male fetus with periventricular nodular heterotopia and filamin A mosaic variant.
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- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 364, doi. 10.1002/pd.6505
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- Publication type:
- Article
Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20C.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 3, p. 369, doi. 10.1002/pd.6506
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- Publication type:
- Article