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Prenatal Diagnosis|July 1, 1985
Exclusion of citrullinaemia in the first trimester of pregnancy by direct assay of argininosuccinate synthetase in chorionic villiE Christensen, N J Brandt, J Philip, et al.Prenatal Diagnosis|January 4, 2026
Gene List Selection Matters: Missed Diagnoses in Prenatal Exome Sequencing-PanelApp R21 and HPO-Driven Versus OMIM-Based Gene ListsVictoria Ardiles-Ruesjas, Laia Rodriguez-Revenga, Montse Pauta, et al.Prenatal Diagnosis|May 1, 1995
The role of percutaneous umbilical blood sampling in the management of immune thrombocytopenic purpuraS H Garmel, S D Craigo, L M Morin, et al.Prenatal Diagnosis|May 1, 1995
Ultrasound observation of amnion dysmorphism at 14.5-16 weeksE Z Zimmer, M BronshteinPrenatal Diagnosis|July 1, 1994
Repeat maternal serum testing in multiple marker Down's syndrome screening programmesH Cuckle, J Densem, N WaldPrenatal Diagnosis|July 1, 1994
Adverse perinatal outcome in patients screen-positive for neural tube defects and fetal Down syndromeS J Gross, O P Phillips, L P Shulman, et al.Prenatal Diagnosis|November 1, 1993
Serum alpha-fetoprotein and neural tube defects in the first trimester of pregnancy. MRC Vitamin Study Research GroupN J Wald, A Hackshaw, R Stone, et al.Prenatal Diagnosis|January 1, 1994
Implications of maternal serum alpha-fetoprotein elevation caused by transabdominal and transcervical CVSS Smidt-Jensen, J Philip, J M Zachary, et al.Prenatal Diagnosis|October 1, 1993
Transabdominal chorionic villus sampling in the second and third trimesters of pregnancy: chromosome quality, reporting time, and feto-maternal bleedingS Smidt-Jensen, C Lundsteen, A M Lind, et al.Prenatal Diagnosis|August 1, 1995
Crown-rump length in aneuploid fetuses: implications for first-trimester biochemical screening for aneuploidiesM C Macintosh, B Brambati, T Chard, et al.Pageof 698