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Prenatal Diagnosis|June 1, 1992
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reactionA Turco, B Peissel, P Quaia, et al.Prenatal Diagnosis|December 24, 2003
Fetal cystoscopy in the management of fetal obstructive uropathy: experience in a single European centreAlec Welsh, Sanjiv Agarwal, Sailesh Kumar, et al.Prenatal Diagnosis|December 24, 2003
Fetal karyotyping after 28 weeks of gestation for late ultrasound findings in a low risk populationC L Drummond, D Molina Gomes, M V Senat, et al.Prenatal Diagnosis|December 24, 2003
First report of prenatal diagnosis of genetic congenital deafness in a routine prenatal genetic testM L Santoro, L Mobili, A Mesoraca, et al.Prenatal Diagnosis|November 25, 2003
Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15A Coulomb L'Herminé, A Aboura, S Brisset, et al.Prenatal Diagnosis|December 10, 2003
Prenatal diagnosis of Apert syndrome: report of two casesDavid L Skidmore, Aditya P Pai, Ants Toi, et al.Prenatal Diagnosis|August 1, 1992
Morphological features of a case of retinoic acid embryopathyL Van Maldergem, E Jauniaux, Y GillerotPrenatal Diagnosis|August 1, 1992
Meconium peritonitis: extrusion of meconium and different sonographical appearances in relation to the stage of the diseaseK Chalubinski, J Deutinger, G BernaschekPrenatal Diagnosis|August 1, 1992
Introduction of early amniocentesis to routine prenatal diagnosisM Djalali, G Barbi, I Kennerknecht, et al.Prenatal Diagnosis|October 27, 2007
Failure of second-trimester measurement of soluble endoglin and other angiogenic factors to predict placental abruptionMinna Tikkanen, Ulf-Håkan Stenman, Mika Nuutila, et al.Pageof 699