Found: 24
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Amniotic fluid alpha-fetoprotein testing in native Japanese women.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 761, doi. 10.1002/(SICI)1097-0223(199908)19:8<761::AID-PD623>3.0.CO;2-I
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Technical factors in early amniocentesis predict adverse outcome. Results of the Canadian early (EA) versus mid-trimester (MA) amniocentesis trial.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 732, doi. 10.1002/(SICI)1097-0223(199908)19:8<732::AID-PD624>3.0.CO;2-N
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Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutations.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 717, doi. 10.1002/(SICI)1097-0223(199908)19:8<717::AID-PD625>3.0.CO;2-L
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Correlation of alkaline phosphatase (ALP) determination and analysis of the tissue non-specific ALP gene in prenatal diagnosis of severe hypophosphatasia.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 755, doi. 10.1002/(SICI)1097-0223(199908)19:8<755::AID-PD629>3.0.CO;2-#
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Precious fertility and third-trimester tests.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 753, doi. 10.1002/(SICI)1097-0223(199908)19:8<753::AID-PD620>3.0.CO;2-S
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Prenatal tests: how are women deciding?
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 743, doi. 10.1002/(SICI)1097-0223(199908)19:8<743::AID-PD636>3.0.CO;2-C
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Variable levels of mosaicism for trisomy 21 in a non-immune hydropic infant with chylothorax.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 764, doi. 10.1002/(SICI)1097-0223(199908)19:8<764::AID-PD618>3.0.CO;2-1
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Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2).
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 783, doi. 10.1002/(SICI)1097-0223(199908)19:8<783::AID-PD635>3.0.CO;2-3
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Prenatal diagnosis of a familial form of junctional ectopic tachycardia.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 767, doi. 10.1002/(SICI)1097-0223(199908)19:8<767::AID-PD617>3.0.CO;2-1
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Comparison of nuchal translucency measurement and second-trimester triple serum screening in twin versus singleton pregnancies.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 727, doi. 10.1002/(SICI)1097-0223(199908)19:8<727::AID-PD631>3.0.CO;2-T
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Second-trimester pregnancy associated plasma protein-A levels are reduced in Cornelia de Lange syndrome pregnancies.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 706, doi. 10.1002/(SICI)1097-0223(199908)19:8<706::AID-PD613>3.0.CO;2-W
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Prenatal ultrasound detection of congenital cataract in trisomy 21.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 780, doi. 10.1002/(SICI)1097-0223(199908)19:8<780::AID-PD634>3.0.CO;2-9
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Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion of uniparental disomy for chromosome 15.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 721, doi. 10.1002/(SICI)1097-0223(199908)19:8<721::AID-PD616>3.0.CO;2-M
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Fetal nuchal translucency and prenatal diagnosis of β -thalassaemia.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 758, doi. 10.1002/(SICI)1097-0223(199908)19:8<758::AID-PD622>3.0.CO;2-H
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Feasibility of prenatal diagnosis of lysinuric protein intolerance by linkage analysis: a case report.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 771, doi. 10.1002/(SICI)1097-0223(199908)19:8<771::AID-PD612>3.0.CO;2-J
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Dimerization of urinary β-core/hCFβcf: a cause of poor β-core assay performance in Down syndrome screening studies.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 790, doi. 10.1002/(SICI)1097-0223(199908)19:8<790::AID-PD627>3.0.CO;2-Z
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Antenatal minimal hydronephrosis: is its follow-up an unnecessary cause of concern?
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 701, doi. 10.1002/(SICI)1097-0223(199908)19:8<701::AID-PD621>3.0.CO;2-5
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Low maternal serum PAPP-A and fetal viability.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 788, doi. 10.1002/(SICI)1097-0223(199908)19:8<788::AID-PD609>3.0.CO;2-Q
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Prenatal ultrasound detection of a congenital epulis in a triple X female fetus: a case report.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 774, doi. 10.1002/(SICI)1097-0223(199908)19:8<774::AID-PD615>3.0.CO;2-7
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Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 739, doi. 10.1002/(SICI)1097-0223(199908)19:8<739::AID-PD626>3.0.CO;2-A
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Inhibin A and non-Down syndrome aneuploidy.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 787, doi. 10.1002/(SICI)1097-0223(199908)19:8<787::AID-PD608>3.0.CO;2-U
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Elective cytogenetic amniocentesis in the third trimester for pregnancies with high risk factors.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 749, doi. 10.1002/(SICI)1097-0223(199908)19:8<749::AID-PD619>3.0.CO;2-#
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Fetal brain death and Dandy-Walker malformation.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 777, doi. 10.1002/(SICI)1097-0223(199908)19:8<777::AID-PD632>3.0.CO;2-B
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Preferences of women facing a prenatal diagnostic choice: long-term outcomes matter most.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 711, doi. 10.1002/(SICI)1097-0223(199908)19:8<711::AID-PD614>3.0.CO;2-V
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