Found: 27
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Prenatal diagnosis of free sialic acid storage disorders (SASD).
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 655, doi. 10.1002/pd.1431
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- Article
Elevated maternal serum alpha-fetoprotein, umbilical vein varix, and mesenchymal dysplasia: are they related?
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 659, doi. 10.1002/pd.1436
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- Article
Prenatal diagnostic indicators of paternal uniparental disomy 14.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 662, doi. 10.1002/pd.1453
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- Article
Variation in the decision to terminate pregnancy in the setting of fetal aneuploidy.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 667, doi. 10.1002/pd.1462
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- Article
First- and second-trimester Down syndrome screening markers in pregnancies achieved through assisted reproductive technologies (ART): a FASTER trial study.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 672, doi. 10.1002/pd.1469
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- Article
Prenatal diagnosis of Freeman-Sheldon syndrome and usefulness of an ultrasound fetal lip width normogram.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 679, doi. 10.1002/pd.1470
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First trimester diagnosis of sirenomelia.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 684, doi. 10.1002/pd.1479
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- Article
Maternal serum ADAM12 levels in Down and Edwards' syndrome pregnancies at 9-12 weeks' gestation.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 689, doi. 10.1002/pd.1480
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- Article
Fetal abdomino-perineal lymphangioma: differential diagnosis and management.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 692, doi. 10.1002/pd.1481
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- Article
Prenatal Marfan syndrome: report of one case and review of the literature.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 696, doi. 10.1002/pd.1482
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- Article
Prenatal diagnosis of absent right and persistent left superior vena cava.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 700, doi. 10.1002/pd.1483
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- Article
First-trimester examination of fetal nasal bone in the Chinese population.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 703, doi. 10.1002/pd.1484
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- Article
Outcome of fetal cerebral posterior fossa anomalies.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 707, doi. 10.1002/pd.1485
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- Article
Multi-centre first-trimester screening for Down syndrome in the Netherlands in routine clinical practice.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 711, doi. 10.1002/pd.1486
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- Article
Carrier diagnostics and prevention of hemoglobinopathies in early pregnancy in The Netherlands: a pilot study.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 719, doi. 10.1002/pd.1490
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- Article
Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3→q31.3) associated with Gorlin syndrome.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 725, doi. 10.1002/pd.1496
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- Article
Repeated measurement of pregnancy-associated plasma protein-A (PAPP-A) in Down syndrome screening: A validation study.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 730, doi. 10.1002/pd.1497
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- Article
Diagnosis and prognosis of fetuses with double outlet right ventricle.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 740, doi. 10.1002/pd.1500
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- Article
Partial tetrasomy chromosome 14. A new prenatal diagnosis case.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 746, doi. 10.1002/pd.1465
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- Article
False-positive diagnosis of intrauterine herpes simplex type 1 infection using PCR.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 749, doi. 10.1002/pd.1466
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- Article
Second-trimester diagnosis of mucopolysaccharidosis type IV a presenting as hydrops fetalis.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 750, doi. 10.1002/pd.1467
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- Article
Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2→qter).
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 752, doi. 10.1002/pd.1488
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Double aneuploid mosaicism 45,X/46,XX/47,XX,+18 in a fetus with cerebral malformations.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 755, doi. 10.1002/pd.1489
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- Article
Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→ter→qter).
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 757, doi. 10.1002/pd.1491
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Two independent rare events-a mutation in the RUNX2 gene and a de novo balanced translocation-in a fetus with cleidocranial dysplasia: pitfall in prenatal diagnosis.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 759, doi. 10.1002/pd.1499
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- Article
Prenatal diagnosis may represent a point of entry of genetic science in sub-Saharan Africa: a survey on the attitudes of medical students and physicians from Cameroon.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 760, doi. 10.1002/pd.1502
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Current awareness in prenatal diagnosis.
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- Prenatal Diagnosis, 2006, v. 26, n. 8, p. 762, doi. 10.1002/pd.1333
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- Article