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Prenatal Diagnosis|November 28, 2002
Strategies for the isolation and detection of fetal cells in transcervical samplesCecilia Bussani, Riccardo Cioni, Benedetta Scarselli, et al.
Prenatal Diagnosis|December 1, 1992
The outcome of pregnancy and prenatal chromosomal diagnosis of fetuses in couples including a translocation carrierS Uehara, T Takabayashi, K Okamura, et al.
Prenatal Diagnosis|December 1, 1992
Fetal granulocytes in maternal venous blood detected by in situ hybridizationM Wessman, K Ylinen, S Knuutila
Prenatal Diagnosis|July 18, 2003
Prenatal diagnosis of triple X using fetal cells obtained by endocervical lavageXiao Xi Zhao, Kaoru Suzumori, Takeshi Sato
Prenatal Diagnosis|July 18, 2003
Histopathological findings of the nose of Down syndrome abortusesS F Wong, W F Ng, L C Ho
Prenatal Diagnosis|July 18, 2003
Residual risk for cytogenetic abnormalities after prenatal diagnosis by interphase fluorescence in situ hybridization (FISH)Jeanne Homer, Sucheta Bhatt, Bing Huang, et al.
Prenatal Diagnosis|July 18, 2003
Prenatal diagnosis of 5p deletion syndrome following abnormally low maternal serum human chorionic gonadotrophinAmir Weiss, Stavit Shalev, Ehud Weiner, et al.
Prenatal Diagnosis|July 18, 2003
Increased total cell-free DNA in the serum of pregnant women carrying a fetus affected by trisomy 21Kevin Spencer, J B de Kok, D W Swinkels
Prenatal Diagnosis|July 18, 2003
Combined first- and second-trimester screening for Down syndrome: an evaluation of proMBP as a markerLine Rode, Karen R Wøjdemann, Anne-Cathrine Shalmi, et al.
Prenatal Diagnosis|December 1, 1992
Prenatal diagnosis of Pallister-Killian syndrome: resolution of cytogenetic ambiguity by use of fluorescent in situ hybridizationS McLean, W Stanley, H Stern, et al.
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