Quantitative fluorescence polymerase chain reaction for the rapid prenatal detection of common aneuploidies and fetal sex

American Journal of Obstetrics and Gynecology

Volumn 177, Issue 4, 1997, Pages 899-906

  Pertl, B ^a   Kopp, S ^a   Kroisel, P M ^a   Hausler, M ^a   Sherlock, J ^a   Winter, R ^a   Adinolfi, M ^a  

^a UNIVERSITY OF GRAZ   (Austria)

Author keywords

PCR; Prenatal diagnosis; Quantitative fluorescence polymerase chain reaction; Trisomy

Indexed keywords

ANEUPLOIDY; ARTICLE; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 19; CHROMOSOME 21; FETUS; FLUORESCENCE; HUMAN; HUMAN TISSUE; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY; X CHROMOSOME;

EID: 0030665915     PISSN: 00029378     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9378(97)70292-8     Document Type: Article

References (24)

1. AF Davies L Barber M Murer-Orlando M Bobrow M. Adinolfi FISH detection of trisomy 21 in interphase by the simultaneous use of two differentially labelled cosmid contigs J Med Genet 31 1994 679 685
2. GL Mutter RJ. Pomponio Molecular diagnosis of sex chromosome aneuploidy using quantitative PCR Nucleic Acids Res 19 1991 4203 4207
3. MB Petersen AA Schinzel F Binkert L Tranebjaerg M Mikkelsen FA Collins Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome Am J Hum Genet 48 1991 65 71
4. A Edwards A Civitello HA Hammond CT. Caskey DNA typing and genetic mapping with trimeric and tetrameric tandem repeats Am J Hum Genet 49 1991 746 756
5. F von Eggeling M Freytag R Fahsold B Horsthemke U. Claussen Rapid detection of trisomy 21 by quantitative PCR Hum Genet 91 1993 567 570
6. ES. Mansfield Diagnosis of Down syndrome and other aneuploidies using quantitative polymerase chain reaction and small tandem repeat polymorphisms Hum Mol Genet 2 1993 43 50
7. B Pertl SC Yau J Sherlock AF Davies CG Mathew M. Adinolfi Rapid molecular method for prenatal detection of Down's syndrome Lancet 343 1994 1197 1198
8. M Adinolfi J Sherlock B. Pertl Rapid detection of selected aneuploidies by quantitative fluorescent PCR Bioessays 17 1995 661 664
9. B Pertl U Weitgasser S Kopp PM Kroisel J Sherlock M. Adinolfi Rapid detection of trisomies 21 and 18 and sexing by quantitative fluorescent multiplex PCR Hum Genet 98 1996 55 59
10. PM Sinet D Theophile Z Rahmani Z Chettouh JL Blouin M Prieur Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level Biomed Pharmacother 48 1994 247 252
11. J Sambrook EF Fritsch T. Maniatis Molecular cloning: a laboratory manual 2nd ed 1989 Cold Spring Harbor Laboratory Press Cold Spring Harbor (MD)
12. MH Polymeropoulos H Xiao CR. Merril Tetranucleotide repeat polymorphism at the human myelin basic protein gene (MBP) Hum Mol Genet 1 1992 658
13. KB Boylan TM Ayres B Popko N Takahashi LE Hood SB Prusiner Repetitive DNA (TGGA)n 5′ to the human myelin basic protein gene: a new form of oligonucleotide repetitive sequence showing length polymorphism Genomics 6 1990 16 22
14. Y Nakahori K Hamano M Iwaya Y. Nakagome Sex identification by polymerase chain reaction using X-Y homologous primer Am J Med Genet 39 1991 472 473
15. MA Aldred T Flint R Vossen K Wakefield MA Ferguson Smith M Lush The EUROGEM map of human chromosome X Eur J Hum Genet 2 1994 248 249
16. Utah Marker Development Group A collection of ordered tetranucleotide-repeat markers from the human genome Am J Hum Genet 57 1995 619 628
17. V Sharma M. Litt Tetranucleotide repeat polymorphism at the D21S11 locus Hum Mol Genet 1 1992 67
18. L Boghosian Sell R Mewar W Harrison RM Shapiro EH Zackai J Carey Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18 Am J Hum Genet 55 1994 476 483
19. K Klinger G Landes D Shook R Harvey L Lopez P Locke Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH) Am J Hum Genet 51 1992 55 65
20. M Adinolfi J Sherlock P Soothill C. Rodeck Molecular evidence of fetal-derived chromosome 21 markers (STRs) in transcervical samples Prenat Diagn 15 1995 35 39
21. A Massari G Novelli A Colosimo F Sangiuolo G Palka G Calabrese Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells Hum Genet 97 1996 150 155
22. W Holzgreve HS Garritsen D. Ganshirt Ahlert Fetal cells in the maternal circulation J Reprod Med 37 1992 410 418
23. DW Bianchi AP Shuber MA DeMaria AC Fougner KW. Klinger Fetal cells in maternal blood: determination of purity and yield by quantitative polymerase chain reaction Am J Obstet Gynecol 171 1994 922 926
24. JL Simpson DE Lewis FZ Bischoff S Elias Isolating fetal nucleated red blood cells from maternal blood: the Baylor experience—1995 Prenat Diagn 15 1995 907 912