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Prenatal Diagnosis|March 1, 2000
Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmationJ L Hand, V V Michels, M J Marinello, et al.
Prenatal Diagnosis|March 1, 2000
Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS)N Kohlschmidt, J Zielinski, E Brude, et al.
Prenatal Diagnosis|March 17, 2000
Critical reappraisal of the utility of sonographic fetal femur length in the prediction of trisomy 21P Vergani, A Locatelli, M G Piccoli, et al.
Prenatal Diagnosis|March 17, 2000
Prenatal control of severe thalassaemia: Chiang Mai strategyT Tongsong, C Wanapirak, P Sirivatanapa, et al.
Prenatal Diagnosis|July 29, 2000
FISH analysis on day 5 post-insemination of human arrested and blastocyst stage embryosP Ruangvutilert, J D Delhanty, P Serhal, et al.
Prenatal Diagnosis|July 29, 2000
Selection of the most common chromosome abnormalities in oocytes prior to ICSIS Munné, S Sepulveda, J Balmaceda, et al.
Prenatal Diagnosis|October 16, 1999
A retrospective evaluation of second-trimester serum screening for fetal trisomy 18: experience of two laboratoriesU Sancken, I Bartels, F Louwen, et al.
Prenatal Diagnosis|October 16, 1999
Second-trimester maternal serum analyte levels associated with fetal trisomy 13D N Saller, J A Canick, M G Blitzer, et al.
Prenatal Diagnosis|February 8, 2000
A widely applicable strategy for single cell genotyping of beta-thalassaemia mutations using DGGE analysis: application to preimplantation genetic diagnosisC Vrettou, G Palmer, E Kanavakis, et al.
Prenatal Diagnosis|February 8, 2000
Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGGK Sermon, S Seneca, A Vanderfaeillie, et al.
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