Found: 23
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An evaluation of the Factor V Leiden mutation in a cohort of African-American pregnant women.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 315, doi. 10.1002/(SICI)1097-0223(199804)18:4<315::AID-PD269>3.0.CO;2-6
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Preliminary evidence for associations between second-trimester human chorionic gonadotropin and unconjugated oestriol levels with pregnancy outcome in Down syndrome pregnancies.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 319, doi. 10.1002/(SICI)1097-0223(199804)18:4<319::AID-PD261>3.0.CO;2-Q
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Intrauterine transfusions influence fetal leukocyte counts and subsets.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 325, doi. 10.1002/(SICI)1097-0223(199804)18:4<325::AID-PD268>3.0.CO;2-6
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Membrane thickness and PROM-high-frequency ultrasound measurements.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 333, doi. 10.1002/(SICI)1097-0223(199804)18:4<333::AID-PD264>3.0.CO;2-H
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Fetal intrahepatic hyperechogenic foci: prenatal ultrasound diagnosis and outcome.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 339, doi. 10.1002/(SICI)1097-0223(199804)18:4<339::AID-PD265>3.0.CO;2-8
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Clinical significance of amniotic-fluid-cell culture failure.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 343, doi. 10.1002/(SICI)1097-0223(199804)18:4<343::AID-PD273>3.0.CO;2-G
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- Article
Awareness and use of prenatal diagnosis among Greek women: a national survey.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 349, doi. 10.1002/(SICI)1097-0223(199804)18:4<349::AID-PD272>3.0.CO;2-D
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Prenatal sonographic diagnosis of skeletal dysplasias-a report of the diagnostic and prognostic accuracy in 35 cases.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 357, doi. 10.1002/(SICI)1097-0223(199804)18:4<357::AID-PD276>3.0.CO;2-0
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B19 parvovirus induced fetal hydrops: rapid and simple diagnosis by detection of B19 antigens in amniotic fluids.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 363, doi. 10.1002/(SICI)1097-0223(199804)18:4<363::AID-PD310>3.0.CO;2-M
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Prenatal diagnosis of Smith-Lemli-Opitz syndrome.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 369, doi. 10.1002/(SICI)1097-0223(199804)18:4<369::AID-PD373>3.0.CO;2-1
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Prenatal diagnosis of an epidermal scalp cyst simulating an encephalocoele.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 373, doi. 10.1002/(SICI)1097-0223(199804)18:4<373::AID-PD254>3.0.CO;2-6
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Case report: prenatal diagnosis of diastrophic dysplasia by ultrasound at 21 weeks of gestation in a mother with massive obesity.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 378, doi. 10.1002/(SICI)1097-0223(199804)18:4<378::AID-PD257>3.0.CO;2-T
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Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 384, doi. 10.1002/(SICI)1097-0223(199804)18:4<384::AID-PD263>3.0.CO;2-4
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Detection of translocations involving the Y-chromosome in prospective prenatal screening of common chromosomal aneuploidies by FISH.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 390, doi. 10.1002/(SICI)1097-0223(199804)18:4<390::AID-PD271>3.0.CO;2-A
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- Article
Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 393, doi. 10.1002/(SICI)1097-0223(199804)18:4<393::AID-PD277>3.0.CO;2-Q
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High resolution chromosome analysis and in situ hybridization on amniotic fluid for diagnosis of a cryptic translocation.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 399, doi. 10.1002/(SICI)1097-0223(199804)18:4<399::AID-PD311>3.0.CO;2-4
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Letter. Early amniocentesis versus chorionic villus sampling.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 405, doi. 10.1002/(SICI)1097-0223(199804)18:4<405::AID-PD258>3.0.CO;2-C
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Letter. Authors' reply.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 407, doi. 10.1002/(SICI)1097-0223(199804)18:4<407::AID-PD275>3.0.CO;2-H
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Letter. Prenatal diagnosis of congenital toxoplasmosis by PCR: extended experience.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 407, doi. 10.1002/(SICI)1097-0223(199804)18:4<407::AID-PD259>3.0.CO;2-7
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Letter. Isoenzymes of maternal serum alkaline phosphatase in Down syndrome.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 409, doi. 10.1002/(SICI)1097-0223(199804)18:4<409::AID-PD266>3.0.CO;2-D
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Letter. Prenatal detection of a deletion 22q11 by FISH.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 411, doi. 10.1002/(SICI)1097-0223(199804)18:4<411::AID-PD262>3.0.CO;2-U
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Letter. Prenatal diagnosis of homozygous α-thalassaemia-1.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 411, doi. 10.1002/(SICI)1097-0223(199804)18:4<411::AID-PD267>3.0.CO;2-F
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Letter. The accuracy of assigned risks in maternal serum screening.
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- Prenatal Diagnosis, 1998, v. 18, n. 4, p. 413, doi. 10.1002/(SICI)1097-0223(199804)18:4<413::AID-PD260>3.0.CO;2-Y
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- Article