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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. i, doi. 10.1002/pd.6513
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Issue Information.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1571, doi. 10.1002/pd.6185
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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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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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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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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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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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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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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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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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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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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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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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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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Biallellic variants in CACNA1S cause fetal akinesia sequence, progressive hydrops and stillbirth.
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- Prenatal Diagnosis, 2023, v. 43, n. 13, p. 1678, doi. 10.1002/pd.6471
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Issue Information.
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1483, doi. 10.1002/pd.6184
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- Article
Congenital small bowel obstruction: Prenatal detection and outcome.
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1485, doi. 10.1002/pd.6461
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Prognostic accuracy of factors associated with poor outcome in prenatally diagnosed sacrococcygeal teratoma: A systematic review and meta‐analysis.
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1495, doi. 10.1002/pd.6457
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Optimal timing of delivery for growth restricted fetuses with gastroschisis: A decision analysis.
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1506, doi. 10.1002/pd.6452
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Fetal lung volumes measured by MRI predict pulmonary morbidity among infants with giant omphaloceles.
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1514, doi. 10.1002/pd.6449
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The normal 14–18 gestational weeks "parasagittal complex" view of the fetal brain. A 3D transvaginal neurosonographic study.
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1520, doi. 10.1002/pd.6456
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Agenesis of the corpus callosum: What to tell expecting parents?
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1527, doi. 10.1002/pd.6447
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Screen‐positive rate in cell free DNA screening for trisomy 21.
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1536, doi. 10.1002/pd.6448
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Haplotype‐based noninvasive prenatal diagnosis of methylmalonic acidemia and the discovery of a recurrent pathogenic haplotype associated with c.609G>A.
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1544, doi. 10.1002/pd.6458
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PIEZO1 is the most common monogenic etiology of non‐immune hydrops fetalis detected by prenatal exome sequencing.
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1556, doi. 10.1002/pd.6451
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Prenatal diagnosis of mucopolysaccharidosis type VII facilitating treatment in neonatal period.
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- Prenatal Diagnosis, 2023, v. 43, n. 12, p. 1567, doi. 10.1002/pd.6455
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Issue Information.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1383, doi. 10.1002/pd.6183
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Droplet digital PCR is a cost‐effective method for analyzing long cell‐free DNA in maternal plasma: Application in preeclampsia.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1385, doi. 10.1002/pd.6432
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Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1394, doi. 10.1002/pd.6444
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Factors associated with late gestational age of diagnosis and/or delayed referral of fetuses with major structural malformations: A study in a tertiary care hospital in South India.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1406, doi. 10.1002/pd.6431
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An overview of reproductive carrier screening panels for autosomal recessive and/or X‐linked conditions: How much do we know?
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1416, doi. 10.1002/pd.6434
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Obstetrical outcomes following amniocentesis performed after 24 weeks of gestation: A systematic review and meta‐analysis.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1425, doi. 10.1002/pd.6435
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Imaging and outcomes of fetal adrenal hemorrhage: A systematic review.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1433, doi. 10.1002/pd.6442
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Outcomes of fetal reduction versus expectant management in dichorionic triamniotic triplets.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1442, doi. 10.1002/pd.6437
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Biometric magnetic resonance imaging analysis of fetal brain development in Down syndrome.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1450, doi. 10.1002/pd.6436
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Fetal de novo heterozygous variant in the isocitrate dehydrogenase 1 gene associated with growth restriction, skeletal, cerebral and vascular anomalies.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1459, doi. 10.1002/pd.6433
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Two unrelated fetuses with ITPR1 missense variants and fetal hydrops.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1463, doi. 10.1002/pd.6439
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Identification of two novel MYH3 variants causing different phenotypes in prenatal diagnosis.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1467, doi. 10.1002/pd.6440
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Prenatal diagnosis of PORCN‐related developmental syndrome in a fetus: A novel phenotype.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1472, doi. 10.1002/pd.6438
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Maternal serological screening for cytomegalovirus infection may play an important role nowadays.
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- Prenatal Diagnosis, 2023, v. 43, n. 11, p. 1477, doi. 10.1002/pd.6441
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Issue Information.
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- Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1263, doi. 10.1002/pd.6182
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- Article
Syndromic congenital diaphragmatic hernia: Current incidence and outcome. Analysis from the congenital diaphragmatic hernia study group registry.
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- Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1265, doi. 10.1002/pd.6407
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Lung proliferation is dependent on the duration not the timepoint of tracheal occlusion in nitrofen rats with diaphragmatic hernia.
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- Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1274, doi. 10.1002/pd.6428
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Cx43 regulates mechanotransduction mechanisms in human preterm amniotic membrane defects.
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- Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1284, doi. 10.1002/pd.6429
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Prenatal assessment of pulmonary vasculature development in fetuses with congenital diaphragmatic hernia: A literature review.
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- Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1296, doi. 10.1002/pd.6412
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Prenatal diagnosis of cleft lip and/or palate: What do we tell prospective parents?
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- Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1310, doi. 10.1002/pd.6418
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Non‐invasive prenatal testing (NIPT): Combination of copy number variant and gene analyses using an "in‐house" target enrichment next generation sequencing—Solution for non‐centralized NIPT laboratory?
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- Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1320, doi. 10.1002/pd.6421
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What helps define outcomes in persistent uninterpretable non‐invasive prenatal testing: Maternal factors, fetal fraction or quality scores?
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- Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1333, doi. 10.1002/pd.6423
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