Found: 23
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Evaluation of chorionic villus sampling safety.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 97, doi. 10.1002/(SICI)1097-0223(199902)19:2<97::AID-PD527>3.0.CO;2-B
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- Article
Detection of numerical chromosome aberrations by comparative genomic hybridization.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 100, doi. 10.1002/(SICI)1097-0223(199902)19:2<100::AID-PD468>3.0.CO;2-H
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Smith-Lemli-Opitz syndrome presenting with persisting nuchal oedema and non-immune hydrops.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 105, doi. 10.1002/(SICI)1097-0223(199902)19:2<105::AID-PD471>3.0.CO;2-W
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Prenatal diagnosis and treatment of holocarboxylase synthetase deficiency.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 108, doi. 10.1002/(SICI)1097-0223(199902)19:2<108::AID-PD476>3.0.CO;2-E
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Some caveats in PCR-based prenatal diagnosis on direct amniotic fluid versus cultured amniocytes.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 113, doi. 10.1002/(SICI)1097-0223(199902)19:2<113::AID-PD475>3.0.CO;2-J
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Fetal neurenteric cyst causing hydrops: case report and review of the literature.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 118, doi. 10.1002/(SICI)1097-0223(199902)19:2<118::AID-PD478>3.0.CO;2-5
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Prediction of pre-eclampsia with maternal mid-trimester total renin, inhibin A, AFP and free β-hCG levels.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 122, doi. 10.1002/(SICI)1097-0223(199902)19:2<122::AID-PD491>3.0.CO;2-R
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Prevalence and significance of isolated fetal choroid plexus cysts detected in early pregnancy by transvaginal sonography in women of advanced maternal age.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 128, doi. 10.1002/(SICI)1097-0223(199902)19:2<128::AID-PD489>3.0.CO;2-Z
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Periconceptional use of folic acid amongst women of advanced maternal age.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 132, doi. 10.1002/(SICI)1097-0223(199902)19:2<132::AID-PD482>3.0.CO;2-M
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Prenatal diagnosis and elective termination of Down syndrome in a racially mixed population in Hawaii, 1987-1996.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 136, doi. 10.1002/(SICI)1097-0223(199902)19:2<136::AID-PD479>3.0.CO;2-Z
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Fetal loss in Down syndrome pregnancies.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 142, doi. 10.1002/(SICI)1097-0223(199902)19:2<142::AID-PD486>3.0.CO;2-7
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Urinary free beta hCG, beta core fragment and total oestriol as markers of Down syndrome in the second trimester of pregnancy.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 146, doi. 10.1002/(SICI)1097-0223(199902)19:2<146::AID-PD502>3.0.CO;2-K
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Prenatal diagnosis of unilateral megalencephaly by 2D and 3D ultrasound: a case report.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 159, doi. 10.1002/(SICI)1097-0223(199902)19:2<159::AID-PD470>3.0.CO;2-G
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Prenatal diagnosis of congenital varicella syndrome and detection of varicella-zoster virus in the fetus: a case report.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 163, doi. 10.1002/(SICI)1097-0223(199902)19:2<163::AID-PD483>3.0.CO;2-9
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Prenatal diagnosis of harlequin ichthyosis by the examination of keratinized hair canals and amniotic fluid cells at 19 weeks' estimated gestational age.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 167, doi. 10.1002/(SICI)1097-0223(199902)19:2<167::AID-PD477>3.0.CO;2-V
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Diagnosis of sex and cystic fibrosis status in fetal erythroblasts isolated from cord blood.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 172, doi. 10.1002/(SICI)1097-0223(199902)19:2<172::AID-PD485>3.0.CO;2-1
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First-trimester non-invasive prenatal diagnosis of triploidy.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 175, doi. 10.1002/(SICI)1097-0223(199902)19:2<175::AID-PD524>3.0.CO;2-4
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A fetus with a 90,XX karyotype.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 178, doi. 10.1002/(SICI)1097-0223(199902)19:2<178::AID-PD530>3.0.CO;2-C
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Overwhelming maternal cell contamination in amniotic fluid samples from patients with oligohydramnios can lead to false prenatal interphase FISH results.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 179, doi. 10.1002/(SICI)1097-0223(199902)19:2<179::AID-PD473>3.0.CO;2-1
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Prenatal supernumerary r(16) chromosome characterized by multiprobe FISH with normal pregnancy outcome.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 181, doi. 10.1002/(SICI)1097-0223(199902)19:2<181::AID-PD507>3.0.CO;2-Z
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Successful DNA-based prenatal diagnosis of the 728+1 g→t mutation at the exon 6-intron 6 junction in the carbonic anhydrase II gene.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 182, doi. 10.1002/(SICI)1097-0223(199902)19:2<182::AID-PD474>3.0.CO;2-2
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Confirmation of the chromosome 8p23.1 euchromatic duplication as a variant with no clinical manifestations.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 183, doi. 10.1002/(SICI)1097-0223(199902)19:2<183::AID-PD481>3.0.CO;2-9
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Chromosome instability limited to the aneuploid clone in the Pallister-Killian syndrome: a pitfall in prenatal diagnosis.
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- Prenatal Diagnosis, 1999, v. 19, n. 2, p. 184, doi. 10.1002/(SICI)1097-0223(199902)19:2<184::AID-PD508>3.0.CO;2-T
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