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Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in northern Israel using polymorphic DNA markersA Shalata, H Mandel, C Dorche, et al.Prenatal Diagnosis|March 4, 2000
Fetal 'space-suit' hydrops in the first trimester: differentiating risk for chromosome abnormalities by delineating characteristics of nuchal translucencyL P Shulman, O P Phillips, D S Emerson, et al.Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis in adenylosuccinate lyase deficiencyS Marie, J W Flipsen, M Duran, et al.Prenatal Diagnosis|March 4, 2000
Parental decisions following prenatal diagnosis of sex chromosome aneuploidy: a trend over timeS M Christian, D Koehn, R Pillay, et al.Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis and outcome in sacrococcygeal teratomas: a review of cases between 1992 and 1998V Brace, S R Grant, K J Brackley, et al.Prenatal Diagnosis|October 16, 1999
Collaborative study of maternal urine beta -core human chorionic gonadotrophin screening for Down syndromeH S Cuckle, J A Canick, L H KellnerPrenatal Diagnosis|October 16, 1999
Maternal urine hyperglycosylated hCG in pregnancies with Down syndromeH S Cuckle, S Shahabi, I K Sehmi, et al.Prenatal Diagnosis|October 16, 1999
Sonographic diagnosis of limb reduction defects in a fetus with haemoglobin Bart's disease at 12 weeks of gestationY H Lam, M H TangPrenatal Diagnosis|October 16, 1999
Termination rates after prenatal diagnosis of Down syndrome, spina bifida, anencephaly, and Turner and Klinefelter syndromes: a systematic literature review. European Concerted Action: DADA (Decision-making After the Diagnosis of a fetal Abnormality)C Mansfield, S Hopfer, T M MarteauPrenatal Diagnosis|October 16, 1999
Mohr syndrome in two sisters: prenatal diagnosis in a 22-week-old fetus with post-mortem findings in bothS Balci, G Güler, G Kale, et al.Pageof 697