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- Published in:
- Prenatal Diagnosis, 2023, v. 43, n. 13, p. i, doi. 10.1002/pd.6513
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- Article
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- Published in:
- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1571, doi. 10.1002/pd.6185
- Publication type:
- Article
New ventures for Prenatal Diagnosis.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1573, doi. 10.1002/pd.6486
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Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1574, doi. 10.1002/pd.6483
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- Article
Improving the accuracy of noninvasive prenatal testing through size‐selection between fetal and maternal cfDNA.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1581, doi. 10.1002/pd.6464
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Risk factors for delayed termination of pregnancy following increased nuchal translucency.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1593, doi. 10.1002/pd.6467
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- Article
The new fetal therapy section awaits your research.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1601, doi. 10.1002/pd.6480
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- Article
Simple prenatal imaging predictors for postnatal cerebrospinal fluid diversion surgery in fetuses undergoing in utero surgery for spina bifida.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1605, doi. 10.1002/pd.6453
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- Article
Percutaneous fetal endoscopic third ventriculostomy for severe isolated cerebral ventriculomegaly.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1614, doi. 10.1002/pd.6465
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- Article
Maternal and fetal safety outcomes after in utero stem cell injection: A systematic review.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1622, doi. 10.1002/pd.6459
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- Article
Intrauterine enzyme replacement therapies for lysosomal storage disorders: Current developments and promising future prospects.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1638, doi. 10.1002/pd.6460
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- Article
Fetal macrocephaly: Pathophysiology, prenatal diagnosis and management.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1650, doi. 10.1002/pd.6473
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- Article
Prenatal diagnosis of autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants presented with thick nuchal translucency and cardiac abnormalities.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1662, doi. 10.1002/pd.6462
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- Article
Neu Laxova syndrome and megacystis in the first trimester: Broadening the fetal phenotype.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1666, doi. 10.1002/pd.6463
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- Article
Prenatal diagnosis of Hartsfield syndrome with a novel genetic variant.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1671, doi. 10.1002/pd.6472
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- Article
A novel SMOC1 pathogenic homozygous variant in a fetus with mesomelia of the lower limbs, micrognathia and hypertelorism and an incidental finding of CYP21A2‐related congenital adrenal hyperplasia.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1674, doi. 10.1002/pd.6485
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- Publication type:
- Article
Biallellic variants in CACNA1S cause fetal akinesia sequence, progressive hydrops and stillbirth.
- Published in:
- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1678, doi. 10.1002/pd.6471
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- Article