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Prenatal Diagnosis|October 4, 2000
Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiencyL Faivre, V Cormier-Daire, D Chrétien, et al.
Prenatal Diagnosis|October 4, 2000
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18C P Chen, S R Chern, L F Yeh, et al.
Prenatal Diagnosis|October 4, 2000
Prenatal molecular diagnosis of glutaric aciduria type I by direct mutation analysisC Busquets, M J Coll, B Merinero, et al.
Prenatal Diagnosis|October 4, 2000
Prenatal diagnosis of glycogen storage disease type 1b using denaturing high performance liquid chromatographyC W Lam, S Y Sin, E T Lau, et al.
Prenatal Diagnosis|February 17, 2001
First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiencyP F Ray, N Gigarel, J P Bonnefont, et al.
Prenatal Diagnosis|February 17, 2001
Prenatal diagnosis of a familial Xq deletion in a female fetus: a case reportL Y Brown, M L Alonso, J Yu, et al.
Prenatal Diagnosis|February 17, 2001
Current awareness in prenatal diagnosis
Prenatal Diagnosis|December 13, 2000
Transposition of the great arteries, ventricular septal defect and diaphragmatic hernia in a fetus: the role of prenatal diagnosis in helping to predict postnatal survivalL Noimark, M Sellwood, J Wyatt, et al.
Prenatal Diagnosis|December 13, 2000
Accuracy of prenatal diagnosis for haemoglobin disorders in the UK: 25 years' experienceJ Old, M Petrou, L Varnavides, et al.
Prenatal Diagnosis|February 17, 2001
Preimplantation genetic diagnosis of compound heterozygous mutations leading to ablation of plakophilin-1 (PKP1) and resulting in skin fragility ectodermal dysplasia syndrome: a case reportA R Thornhill, S J Pickering, N V Whittock, et al.
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