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Prenatal Diagnosis|May 1, 1996
Prenatal identification of a heterozygous status in two fetuses at risk for glucose-galactose malabsorptionM G Martín, E Turk, C Kerner, et al.Prenatal Diagnosis|January 1, 1996
Maternal serum screening for fetal Down syndrome in IVF pregnanciesL S Ribbert, L H Kornman, B T De Wolf, et al.Prenatal Diagnosis|November 26, 2016
The role of aberrant methylation of trophoblastic stem cell origin in the pathogenesis and diagnosis of placental disordersBeenish Rahat, Rauf Ahmad Najar, Abid Hamid, et al.Prenatal Diagnosis|July 1, 1989
Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probesM Raux-Demay, E Mornet, J Boue, et al.Prenatal Diagnosis|December 16, 2016
Termination of pregnancy due to renal tract abnormalities: survey of 97 fetuses from a single medical centerYaakov Melcer, Gaby Kaplan, Ido Ben-Ami, et al.Prenatal Diagnosis|December 16, 2016
A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimensSongchang Chen, Deyuan Liu, Junyu Zhang, et al.Prenatal Diagnosis|August 1, 1989
First-trimester prenatal diagnosis of homozygous (14;21) translocation in a fetus with 44 chromosomesB Dallapiccola, G Ferranti, D Altissimi, et al.Prenatal Diagnosis|August 1, 1989
The value of routine cervical cultures before transcervical chorionic villus samplingM J Kagie, P L Petit, H H KanhaiPrenatal Diagnosis|September 1, 1989
First-trimester prenatal diagnosis of aspartylglucosaminuriaP Aula, K Mattila, O Piiroinen, et al.Pageof 698