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Prenatal Diagnosis|July 1, 1996
Prenatal diagnosis by enzyme analysis in 15 pregnancies at risk for the Lesch-Nyhan syndromeG W Graham, D A Aitken, J M ConnorPrenatal Diagnosis|July 1, 1996
In utero congestive heart failure due to maternal indomethacin treatment for polyhydramnios and premature labour in a fetus with antenatal closure of the foramen ovaleR Achiron, S Lipitz, D Kidron, et al.Prenatal Diagnosis|July 1, 1996
The sequential in utero death of heterokaryotic monozygotic twins. A case report and literature reviewA D Weeks, N P Davies, A Sprigg, et al.Prenatal Diagnosis|July 1, 1996
Size disparity of the choroid plexuses of the lateral ventricles: prenatal diagnosis and neonatal outcomeB M Petrikovsky, G P KaplanPrenatal Diagnosis|May 1, 1996
Couple-based prenatal screening for cystic fibrosis in primary care settingsR A Doherty, G E Palomaki, E M Kloza, et al.Prenatal Diagnosis|July 1, 1995
In utero diagnosis and treatment of fetal goitrous hypothyroidism, caused by maternal use of propylthiouracilA J Van Loon, J T Derksen, A F Bos, et al.Prenatal Diagnosis|July 1, 1995
A 10-year survey, 1980-1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12,699 prenatal samplesK Brøndum-Nielsen, M MikkelsenPrenatal Diagnosis|July 1, 1995
The time of appearance and disappearance of fetal DNA from the maternal circulationM R Thomas, B Tutschek, A Frost, et al.Prenatal Diagnosis|July 1, 1995
Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: implications for prenatal diagnosis in one familyJ A McGrath, J R McMillan, M G Dunnill, et al.Prenatal Diagnosis|February 24, 2006
Second-trimester prenatal screening for trisomy 21 using biochemical markers: a 7-year experience in one cytogenetic laboratoryHélène Marical, Nathalie Douet-Guilbert, Karine Bages, et al.Pageof 699