Prenatal detection of chromosome disorders by QF-PCR
- 1 September 2001
- journal article
- editorial
- Published by Elsevier in The Lancet
- Vol. 358 (9287) , 1030-1031
- https://doi.org/10.1016/s0140-6736(01)06229-8
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Assessment of new markers for the rapid detection of aneuploidies by quantitative fluorescent PCR (QF–PCR)Annals of Human Genetics, 2001
- A large‐scale evaluation of amnio‐PCR for the rapid prenatal diagnosis of fetal trisomyUltrasound in Obstetrics & Gynecology, 2001
- Detection of aneuploidy in chromosomes X, Y, 13, 18 and 21 by QF-PCR in 662 selected pregnancies at risk.Molecular Human Reproduction, 2000
- Rapid detection of chromosomes X and Y aneuploidies by quantitative fluorescent PCRPrenatal Diagnosis, 1999
- Rapid and simple prenatal DNA diagnosis of Down's syndromeThe Lancet, 1998
- Assessment of diagnostic quantitative fluorescent multiplex polymerase chain reaction assays performed on single cellsAnnals of Human Genetics, 1998
- Rapid detection of aneuploidies by microsatellite and the quantitative fluorescent polymerase chain reactionPrenatal Diagnosis, 1997
- Quantitative fluorescence polymerase chain reaction for the rapid prenatal detection of common aneuploidies and fetal sexAmerican Journal of Obstetrics and Gynecology, 1997
- DNA Repeats -- A Treasury of Human VariationNew England Journal of Medicine, 1994
- Rapid molecular method for prenatal detection of Down's syndromeThe Lancet, 1994