Found: 19
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Prenatal diagnosis of 21-hydroxylase deficiency caused by gene conversion and rearrangements: pitfalls and molecular diagnostic solutions.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1171, doi. 10.1002/pd.467
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- Article
Prenatal sonographic diagnosis of the 49,XXXXY syndrome.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1177, doi. 10.1002/pd.473
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- Article
Compromise ultrasound dating policy in maternal serum screening for Down syndrome.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1181, doi. 10.1002/pd.474
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- Article
Prenatal ultrasound diagnosis of Toriello-Carey syndrome.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1185, doi. 10.1002/pd.488
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Interpreting information: what is said, what is heard-a questionnaire study of health professionals and members of the public.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1188, doi. 10.1002/pd.489
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- Article
Preference assessment of prenatal diagnosis for Down syndrome: is 35 years a rational cutoff?
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1195, doi. 10.1002/pd.494
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- Article
The association between fetal pyelectasis on second trimester ultrasound scan and aneuploidy among 25 586 low risk unselected women.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1201, doi. 10.1002/pd.490
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- Article
Gender impact on first trimester markers in Down syndrome screening.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1207, doi. 10.1002/pd.493
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- Article
Prenatal diagnosis and treatment of fetal long QT syndrome: a case report.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1209, doi. 10.1002/pd.475
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- Article
Limited expression of Fas and Fas ligand in fetal nucleated erythrocytes isolated from first trimester maternal blood.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1213, doi. 10.1002/pd.480
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- Article
Hypoechogenicity of fetal long bones: a new ultrasound marker for arthrogryposis.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1219, doi. 10.1002/pd.492
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Some observations of the structure of the choroid plexus and its cysts.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1223, doi. 10.1002/pd.486
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- Article
Uptake of prenatal screening for chromosomal anomalies: impact of test results in a previous pregnancy.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1229, doi. 10.1002/pd.504
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- Article
Nuchal index: a gestational age independent ultrasound marker for the detection of Down syndrome.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1233, doi. 10.1002/pd.497
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- Article
Translocation 1q15q in a fetus with holoprosencephaly.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1238, doi. 10.1002/pd.479
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- Article
Trisomy 7 mosaicism: prognosis after prenatal diagnosis.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1239, doi. 10.1002/pd.482
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- Article
Prenatal diagnosis of iniencephaly and alobar holoprosencephaly with trisomy 13 mosaicism: a case report.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1240, doi. 10.1002/pd.484
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- Article
Fetal fibrochondrogenesis at 26 weeks' gestation. Hanitra Randrianaivo, Georges Haddad, Horatiu Roman, Anne Lise Delezoide, Annick Toutain, Martine Le Merrer, Claude Moraine. Prenatal Diagnosis 22(9):806-810.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1241, doi. 10.1002/pd.513
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- Article
First-trimester fetal sex determination in maternal serum using real-time PCR. Jean-Marc Costa, Alexandra Benachi, Evelyne Gautier, Jean-Marie Jouannic, Pauline Ernault, Yves Dume. Prenatal Diagnosis 21(12): 1070-1074.
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- Prenatal Diagnosis, 2002, v. 22, n. 13, p. 1241, doi. 10.1002/pd.512
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- Article