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Prenatal 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.Prenatal Diagnosis|November 9, 2002
Degree of fetal umbilical venous constriction at the abdominal wall in a low-risk population at 20-40 weeks of gestationSvein Magne Skulstad, Torvid Kiserud, Svein RasmussenPrenatal Diagnosis|November 9, 2002
Evaluating the risk of tuberous sclerosis in cases with prenatal diagnosis of cardiac rhabdomyomaRonni Gamzu, Reuven Achiron, Julius Hegesh, et al.Prenatal Diagnosis|November 9, 2002
McKusik-Kaufman syndrome: prenatal diagnosis, genetics and follow upPascal Gaucherand, Chantal Vavasseur-Monot, Elizabeth Ollagnon, et al.Prenatal Diagnosis|January 21, 2003
Assessment of the thymus at echocardiography in fetuses at risk for 22q11.2 deletionCatherine Barrea, Shi-Joon Yoo, David Chitayat, et al.Prenatal Diagnosis|January 21, 2003
Fetal liver hyperechogenicity on sonography may be a serendipitous sign of a transient myeloproliferating disorderAntonella Vimercati, Pantaleo Greco, Antonia Gentile, et al.Prenatal Diagnosis|January 21, 2003
Detection of gamma-globin mRNA in fetal nucleated red blood cells by PNA fluorescence in situ hybridizationRasmus Dines Larsen, Andreas Schønau, Marianne Thisted, et al.Prenatal Diagnosis|December 13, 2000
The subarachnoid space: normal fetal development as demonstrated by transvaginal ultrasoundG Malinger, T Lerman-Sagie, R Achiron, et al.Prenatal Diagnosis|December 13, 2000
Prenatal diagnosis of haemoglobin Bart's disease by cordocentesis at 12-14 weeks--experience with the first 59 casesY H Lam, M H TangPrenatal Diagnosis|December 13, 2000
Prolidase deficiency among an Israeli population: prenatal diagnosis in a genetic disorder with uncertain prognosisH Mandel, N Abeling, A Gutman, et al.Pageof 695