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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 SwinkelsPrenatal 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.Prenatal Diagnosis|December 13, 2002
Prenatal ultrasound diagnosis of Toriello-Carey syndromeDario Paladini, Maria Giovanna Russo, Antonio Tartaglione, et al.Prenatal Diagnosis|December 13, 2002
Uptake of prenatal screening for chromosomal anomalies: impact of test results in a previous pregnancyKevin SpencerPrenatal Diagnosis|November 9, 2002
Pregnancy outcome following prenatal diagnosis of an isodicentric X chromosome: first case reportA Lebbar, G Viot, S Szpiro-Tapia, et al.Prenatal Diagnosis|November 9, 2002
Fetal bradycardia in the first trimester: an unusual presentation of atrial extrasystolesS F Wong, K T Chau, L C HoPrenatal Diagnosis|November 9, 2002
Rapid diagnosis of triploidy of maternal origin using fluorescent PCR and DNA fragment analysis in the third trimester of pregnancyZoltán Bán, Bálint Nagy, Csaba Papp, et al.Pageof 695