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Prenatal Diagnosis|January 1, 1983
Mid-trimester fetal ultrasound: diagnostic dilemmasV L Corson, R C Sanders, T R Johnson, et al.Prenatal Diagnosis|January 1, 1983
Prenatal diagnosis, fetal pathology and cytogenetic analysis of a 46,XX/47,XX, + 15 mosaicG Gimelli, C Cuoco, E Porro, et al.Prenatal Diagnosis|August 14, 2016
An exploration of the potential utility of fetal cardiovascular MRI as an adjunct to fetal echocardiographyDavid F A Lloyd, Joshua F P van Amerom, Kuberan Pushparajah, et al.Prenatal Diagnosis|November 1, 1984
A culture vessel for amniotic fluid cells allowing faster preparation of chromosome slidesA Tabor, A M Lind, A M Andersen, et al.Prenatal Diagnosis|November 1, 1984
Pericentric inversion of the Y chromosome and prenatal diagnosisL R Shapiro, R O Pettersen, P L Wilmot, et al.Prenatal Diagnosis|July 1, 1984
Selective survival of only the healthy fetus following prenatal diagnosis of thalassaemia major in binovular twin gestationA Antsaklis, J Politis, C Karagiannopoulos, et al.Prenatal Diagnosis|July 1, 1984
Prenatal diagnosis of a 46,XX/47,XX, + 12 mosaicP K Jensen, N Hahnemann, H Rehder, et al.Prenatal Diagnosis|July 1, 1984
Amniotic band syndrome in second trimester associated with fetal malformationsK G BørlumPrenatal Diagnosis|July 1, 1981
Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency by steroid analysis in the amniotic fluid of mid-pregnancy: comparison with HLA typing in 17 pregnancies at risk for CAHM G Forest, H Bétuel, P Couillin, et al.Prenatal Diagnosis|January 1, 1981
Prenatal diagnosis of congenital adrenal hyperplasia (21-OH deficiency type) by HLA typingP Couillin, J Boue, H Nicolas, et al.Pageof 698