Found: 21
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Appropriate biochemical parameters in first-trimester screening for Down syndrome.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 505, doi. 10.1002/(SICI)1097-0223(199906)19:6<505::AID-PD572>3.0.CO;2-6
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A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 570, doi. 10.1002/(SICI)1097-0223(199906)19:6<570::AID-PD582>3.0.CO;2-Q
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High failure rate of umbilical vessel occlusion by ultrasound-guided injection of absolute alcohol or enbucrilate gel.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 527, doi. 10.1002/(SICI)1097-0223(199906)19:6<527::AID-PD576>3.0.CO;2-N
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First-trimester diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) using PPT enzyme assay and CLN1 mutation analysis.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 559, doi. 10.1002/(SICI)1097-0223(199906)19:6<559::AID-PD587>3.0.CO;2-8
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Fetal cardiac abnormalities and their association with aneuploidy.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 563, doi. 10.1002/(SICI)1097-0223(199906)19:6<563::AID-PD605>3.0.CO;2-M
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Trisomy 18 with total cranio-rachischisis and thoraco-abdominoschisis.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 580, doi. 10.1002/(SICI)1097-0223(199906)19:6<580::AID-PD583>3.0.CO;2-K
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Molecular prenatal diagnosis of ataxia telangiectasia heterozygosity by direct mutational assays.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 542, doi. 10.1002/(SICI)1097-0223(199906)19:6<542::AID-PD586>3.0.CO;2-L
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Maternal serum activin A and follistatin levels in pregnancies with Down syndrome.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 513, doi. 10.1002/(SICI)1097-0223(199906)19:6<513::AID-PD579>3.0.CO;2-L
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Haemolytic disease of the newborn caused by anti-c, anti-E and anti-Fya antibodies: report of five cases.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 533, doi. 10.1002/(SICI)1097-0223(199906)19:6<533::AID-PD570>3.0.CO;2-5
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Prenatal diagnosis of tuberous sclerosis with intracerebral signs at 14 weeks' gestation.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 575, doi. 10.1002/(SICI)1097-0223(199906)19:6<575::AID-PD580>3.0.CO;2-R
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Prenatal detection of a giant bilateral thoracic vascular lesion: prognostic evaluation and genetic aspects.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 583, doi. 10.1002/(SICI)1097-0223(199906)19:6<583::AID-PD585>3.0.CO;2-B
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Evolution of the centromeric alpha-satellite DNA sequences of human chromosome 22.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 590, doi. 10.1002/(SICI)1097-0223(199906)19:6<590::AID-PD567>3.0.CO;2-7
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A comparison of different density gradients and antibodies for enrichment of fetal erythroblasts by MACS.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 521, doi. 10.1002/(SICI)1097-0223(199906)19:6<521::AID-PD578>3.0.CO;2-N
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Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 546, doi. 10.1002/(SICI)1097-0223(199906)19:6<546::AID-PD589>3.0.CO;2-8
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The prenatal diagnosis of Pierre-Robin sequence.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 567, doi. 10.1002/(SICI)1097-0223(199906)19:6<567::AID-PD581>3.0.CO;2-P
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SP1 in pregnancies with Down syndrome in the first trimester of pregnancy.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 517, doi. 10.1002/(SICI)1097-0223(199906)19:6<517::AID-PD591>3.0.CO;2-2
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The association of increased fetal nuchal translucency and spinal muscular atrophy type I.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 587, doi. 10.1002/(SICI)1097-0223(199906)19:6<587::AID-PD584>3.0.CO;2-A
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Maternal serum screening for Down syndrome in the first trimester: experience from Belarus.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 499, doi. 10.1002/(SICI)1097-0223(199906)19:6<499::AID-PD555>3.0.CO;2-6
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Complex approach to prenatal diagnosis of cytochrome c oxidase deficiencies.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 552, doi. 10.1002/(SICI)1097-0223(199906)19:6<552::AID-PD588>3.0.CO;2-C
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Inconsistency of omphalocoele contents in three consecutive siblings with partial trisomy 3q and partial monosomy 11q.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 591, doi. 10.1002/(SICI)1097-0223(199906)19:6<591::AID-PD577>3.0.CO;2-5
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Maternal serum pregnancy-associated plasma protein A (PAPP-A) but not pregnancy-specific β1-glycoprotein (SP1) is a useful second-trimester marker for fetal trisomy 18.
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- Prenatal Diagnosis, 1999, v. 19, n. 6, p. 537, doi. 10.1002/(SICI)1097-0223(199906)19:6<537::AID-PD573>3.0.CO;2-T
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