Showing results (801-810 of 6,980) with videos related to
Sort By:
Pageof 698
Prenatal Diagnosis|August 12, 2004
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal surveyA Sensi, S Cavani, N Villa, et al.Prenatal Diagnosis|May 1, 1992
First-trimester biochemical and molecular diagnoses using chorionic villi: high accuracy in the U.S. collaborative studyR J Desnick, J L Schuette, M S Golbus, et al.Prenatal Diagnosis|May 1, 1992
The risk and efficacy of chorionic villus sampling in multiple gestationsE Pergament, J D Schulman, K Copeland, et al.Prenatal Diagnosis|August 10, 2004
Congenital diaphragmatic hernia: prenatal diagnosis permits immediate intensive care with high survival rate in isolated cases. A population-based studyPierre Bétrémieux, Théophile Gaillot, Armelle de la Pintière, et al.Prenatal Diagnosis|August 10, 2004
Alphafoetoprotein and acetylcholinesterase in amniotic fluid as a factor suggesting fetal skin and nerve lesions in a case of congenital varicella syndromeVéronique Mirlesse, Nathalie Duguy, Evelyne Cynober, et al.Prenatal Diagnosis|August 10, 2004
Efficacy and clinical outcome of preimplantation genetic diagnosis using FISH for couples of reciprocal and Robertsonian translocations: the Korean experienceChun Kyu Lim, Jin Hyun Jun, Dong Mi Min, et al.Prenatal Diagnosis|August 10, 2004
Duplex, triplex and quadruplex PCR for the preimplantation genetic diagnosis (PGD) of cystic fibrosis (CF), an exhaustive approachCéline Moutou, Nathalie Gardes, Stéphane VivillePrenatal Diagnosis|May 1, 1992
Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. chromosome mosaicism in CVS and amniocentesis samplesI E Teshima, D K Kalousek, M J Vekemans, et al.Prenatal Diagnosis|June 21, 2005
The prenatal multiplier method for prediction of limb length discrepancyJonathan Paley, Amanda Gelman, Dror Paley, et al.Prenatal Diagnosis|June 21, 2005
Prospective audit of a one-centre combined nuchal translucency and triple test programme for the detection of trisomy 21Vijayalakshmi Babbur, Christoph C Lees, Sandra F Goodburn, et al.Pageof 698