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Prenatal Diagnosis|May 18, 1999
The use of in vitro expanded erythroid cells in a model system for the isolation of fetal cells from maternal bloodM W Jansen, M von Lindern, H Beug, et al.Prenatal Diagnosis|May 18, 1999
Urinary screening tests for fetal Down syndrome: I. Fresh beta-core fragmentL A Cole, K M Rinne, S M Mahajan, et al.Prenatal Diagnosis|May 18, 1999
First-trimester screening for Down syndrome using nuchal translucency measurement with free beta-hCG and PAPP-A between 10 and 13 weeks of pregnancy--the combined testP De Biasio, M Siccardi, G Volpe, et al.Prenatal Diagnosis|May 18, 1999
Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiencyK M Brookhyser, M H Lipson, A B Moser, et al.Prenatal Diagnosis|October 4, 2000
The Genoa experience of prenatal diagnosis in NF1P Origone, E Bonioli, E Panucci, et al.Prenatal Diagnosis|May 23, 2000
Screening for trisomies 21 and 18 with maternal serum placental isoferritin p43 componentC Moroz, R Maymon, E Jauniaux, et al.Prenatal Diagnosis|May 23, 2000
Prenatal diagnosis of alobar holoprosencephaly by two-dimensional and three-dimensional ultrasoundT H Lai, C H Chang, C H Yu, et al.Prenatal Diagnosis|May 23, 2000
The use of transferrin for enrichment of fetal cells from maternal bloodM Serlachius, H Von Koskull, M Wessman, et al.Prenatal Diagnosis|May 23, 2000
Prenatal ultrasound of regional akinesia with Pena-Shokier phenotypeT Tongsong, P Chanprapaph, S KhunamornpongPrenatal Diagnosis|October 4, 2000
Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiencyL Faivre, V Cormier-Daire, D Chrétien, et al.Pageof 698