Showing results (451-460 of 6,945) with videos related to
Sort By:
Pageof 695
Prenatal Diagnosis|July 29, 2000
FISH analysis on day 5 post-insemination of human arrested and blastocyst stage embryosP Ruangvutilert, J D Delhanty, P Serhal, et al.Prenatal Diagnosis|July 29, 2000
Selection of the most common chromosome abnormalities in oocytes prior to ICSIS Munné, S Sepulveda, J Balmaceda, et al.Prenatal Diagnosis|October 16, 1999
A retrospective evaluation of second-trimester serum screening for fetal trisomy 18: experience of two laboratoriesU Sancken, I Bartels, F Louwen, et al.Prenatal Diagnosis|October 16, 1999
Second-trimester maternal serum analyte levels associated with fetal trisomy 13D N Saller, J A Canick, M G Blitzer, et al.Prenatal Diagnosis|February 8, 2000
A widely applicable strategy for single cell genotyping of beta-thalassaemia mutations using DGGE analysis: application to preimplantation genetic diagnosisC Vrettou, G Palmer, E Kanavakis, et al.Prenatal Diagnosis|February 8, 2000
Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGGK Sermon, S Seneca, A Vanderfaeillie, et al.Prenatal Diagnosis|June 9, 1999
Low levels of natural killer cells in pregnant women transmitting Toxoplasma gondiiG Nigro, J Piazze, R Paesano, et al.Prenatal Diagnosis|June 9, 1999
A role for maternal serum screening in detecting chromosomal abnormalities in fetuses with isolated choroid plexus cysts: a prospective multicentre studyT Brown, M A Kliewer, B S Hertzberg, et al.Prenatal Diagnosis|June 9, 1999
Insights into the pathogenesis and natural history of fetuses with multicystic dysplastic kidney diseaseN Lazebnik, M F Bellinger, J E Ferguson, et al.Prenatal Diagnosis|June 9, 1999
RhD status of a fetus at risk for haemolytic disease with a discrepant maternal DNA-based RhD genotypeG A Denomme, H Akoury, M Sermer, et al.Pageof 695