Found: 20
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Current awareness in prenatal diagnosis.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. i, doi. 10.1002/pd.2355
- Publication type:
- Article
Maternal plasma soluble fms-like tyrosine kinase-1 and free vascular endothelial growth factor at 11 to 13 weeks of gestation in preeclampsia.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 191, doi. 10.1002/pd.2433
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- Publication type:
- Article
Trends in prenatal screening and diagnostic testing among women referred for advanced maternal age.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 198, doi. 10.1002/pd.2434
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- Publication type:
- Article
Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 207, doi. 10.1002/pd.2437
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- Publication type:
- Article
Maternal serum human placental growth hormone at 11 to 13 weeks in trisomy 21 and trisomy 18 pregnancies.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 212, doi. 10.1002/pd.2438
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- Publication type:
- Article
Hypertensive disorders in pregnancy: combined screening by uterine artery Doppler, blood pressure and serum PAPP-A at 11-13 weeks.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 216, doi. 10.1002/pd.2440
- By:
- Publication type:
- Article
Maternal plasma levels of follistatin-related gene protein in the first trimester of pregnancies with Down syndrome.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 224, doi. 10.1002/pd.2441
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- Publication type:
- Article
Identification of circulating placental mRNA in maternal blood of pregnancies affected with fetal congenital heart diseases at the second trimester of pregnancy: implications for early molecular screening.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 229, doi. 10.1002/pd.2443
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- Publication type:
- Article
First trimester aneuploidy screening in the presence of a vanishing twin: implications for maternal serum markers.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 235, doi. 10.1002/pd.2445
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- Publication type:
- Article
Effect of religion on the attitude of primiparous women toward genetic testing.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 241, doi. 10.1002/pd.2447
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- Publication type:
- Article
Difference in nuchal translucency between monozygotic and dizygotic spontaneously conceived twins.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 247, doi. 10.1002/pd.2450
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- Publication type:
- Article
Hematological characteristics in neonates with twin anemia-polycythemia sequence (TAPS)
- Published in:
- 2010
- By:
- Publication type:
- Journal Article
Hematological characteristics in neonates with twin anemia-polycythemia sequence (TAPS).
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 251, doi. 10.1002/pd.2453
- By:
- Publication type:
- Article
First-trimester sonographic findings in trisomy 18: a review of 53 cases.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 256, doi. 10.1002/pd.2462
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- Publication type:
- Article
Non-invasive detection and quantification of human foetal brain lactate in utero by magnetic resonance spectroscopy.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 260, doi. 10.1002/pd.2463
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- Publication type:
- Article
Fetal anatomic survey using three-dimensional ultrasound in conjunction with first-trimester nuchal translucency screening.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 267, doi. 10.1002/pd.2446
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- Publication type:
- Article
Pre- and postnatal diagnosis and outcome of fetuses and neonates with esophageal atresia and tracheoesophageal fistula.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 274, doi. 10.1002/pd.2466
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- Publication type:
- Article
Prenatal diagnosis of del(4)(q27q31.23), due to a maternal balanced complex chromosome rearrangement, characterized by array-CGH.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 280, doi. 10.1002/pd.2439
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- Publication type:
- Article
Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 284, doi. 10.1002/pd.2458
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- Publication type:
- Article
Trisomy 18 and 13 screening: consequences for the Dutch Down syndrome screening programme.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 287, doi. 10.1002/pd.2467
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- Publication type:
- Article