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Prenatal Diagnosis|July 27, 1999
Prenatal features of Noonan syndromeD L Nisbet, D R Griffin, L S ChittyPrenatal Diagnosis|July 23, 1999
Appropriate biochemical parameters in first-trimester screening for Down syndromeH S Cuckle, J M van LithPrenatal Diagnosis|July 23, 1999
Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidiesA Morris, E Boyd, S Dhanjal, et al.Prenatal Diagnosis|July 23, 1999
Complex approach to prenatal diagnosis of cytochrome c oxidase deficienciesJ Houstek, P Klement, J Hermanská, et al.Prenatal Diagnosis|July 23, 1999
The prenatal diagnosis of Pierre-Robin sequenceY Y Hsieh, C C Chang, H D Tsai, et al.Prenatal Diagnosis|July 23, 1999
Trisomy 18 with total cranio-rachischisis and thoraco-abdominoschisisS J Donaldson, C A Wright, T J de RavelPrenatal Diagnosis|March 31, 2000
Prenatal ultrasound findings in affected and unaffected pregnancies that are screen-positive for trisomy 18: the California experienceL B Feuchtbaum, R J Currier, F W Lorey, et al.Prenatal Diagnosis|March 31, 2000
DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprintingC C Glenn, G Deng, R C Michaelis, et al.Prenatal Diagnosis|March 31, 2000
The sonographic diagnosis of Dandy-Walker and Dandy-Walker variant: associated findings and outcomesJ L Ecker, T D Shipp, B Bromley, et al.Prenatal Diagnosis|March 31, 2000
Exclusion of late infantile neuronal ceroid lipofuscinosis (LINCL) in a fetus by assay of tripeptidyl peptidase I in chorionic villiE P Young, B G Winchester, W Peter Logan, et al.Pageof 699