Found: 19
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The 'Consecutive Combined Test'-using Double test from week 8 + 0 and Nuchal Translucency Scan, for first trimester screening for Down Syndrome.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1105, doi. 10.1002/pd.1487
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- Article
Prenatal diagnosis of neurofibromatosis type 1: sonographic and MRI findings.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1110, doi. 10.1002/pd.1560
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- Article
Quantitative distribution of a panel of circulating mRNA in preeclampsia versus controls.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1115, doi. 10.1002/pd.1562
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- Article
Prenatal sonographic diagnosis of Malpuech syndrome.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1121, doi. 10.1002/pd.1564
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- Article
Single large study or meta-analysis parameters: choosing the most appropriate tool for Down syndrome screening in the first trimester.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1124, doi. 10.1002/pd.1568
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- Article
Chorionic villus sampling for beta-thalassemia: the first report of experience in Iran.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1131, doi. 10.1002/pd.1572
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- Article
First-trimester maternal dried blood Down syndrome screening marker levels in early pregnancy loss.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1137, doi. 10.1002/pd.1574
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- Article
Supernumerary marker chromosomes detected in 100 000 prenatal diagnoses: molecular cytogenetic studies and clinical significance.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1142, doi. 10.1002/pd.1575
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- Article
A new osteochondrodysplasia with severe osteopenia, preaxial polydactyly, clefting and dysmorphic features resembling filamin-related disorders.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1151, doi. 10.1002/pd.1576
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- Article
Psychological consequences of prenatal diagnosis in a case of familial Angelman Syndrome.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1156, doi. 10.1002/pd.1577
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- Article
Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1160, doi. 10.1002/pd.1582
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- Article
Prenatal diagnosis of trisomy 21 without the Down syndrome phenotype.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1168, doi. 10.1002/pd.1583
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- Article
Gene duplications in 21-hydroxylase deficiency: the importance of accurate molecular diagnosis in carrier detection and prenatal diagnosis.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1172, doi. 10.1002/pd.1584
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- Article
Mosaic trisomy 16 in a fetus: the complex relationship between phenotype and genetic mechanisms.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1179, doi. 10.1002/pd.1585
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- Article
Three stage contingent screening for Down syndrome.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1183, doi. 10.1002/pd.1579
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- Article
De novo chromosomal abnormalities and month of conception. Data from the southern hemisphere.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1184, doi. 10.1002/pd.1586
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- Article
A matter of opinion of evidence!
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1184, doi. 10.1002/pd.1578
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- Article
Limited value of echography to predict true fetal mosaicism for trisomy 12.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1186, doi. 10.1002/pd.1587
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- Article
Current awareness in prenatal diagnosis.
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- Prenatal Diagnosis, 2006, v. 26, n. 12, p. 1190, doi. 10.1002/pd.1337
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- Article