Assessment of new makers for the rapid detection of aneuploidies by quantitative fluorescent PCR (QF-PCR)

Annals of Human Genetics

Volumn 65, Issue 5, 2001, Pages 421-427

  Cirigliano, V ^a,b   Lewin, P ^c   Szpiro Tapies, S ^c   Fuster, C ^c   Adinolfi, M ^d  

^a General Lab   (Spain)

^b UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^c LABORATOIRE CERBA   (France)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMELOGENIN;

ADULT; ALLELE; AMNION FLUID ANALYSIS; ANEUPLOIDY; ARTICLE; AUTOSOME; CELL SUBPOPULATION; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME ARM; CHROMOSOME MARKER; CONTROLLED STUDY; DIAGNOSTIC VALUE; DOWN SYNDROME; FEMALE; FETUS; GENE MAPPING; GENE SEQUENCE; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE 45,X; KARYOTYPE 47,XXY; KARYOTYPE 47,XYY; MALE; MEDICAL ASSESSMENT; NUMERICAL CHROMOSOME ABERRATION; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SEX CHROMOSOME ABERRATION; SEX CHROMOSOME MOSAICISM; SEX DETERMINATION; TANDEM REPEAT; TRISOMY; TURNER SYNDROME; X CHROMOSOME; X CHROMOSOME LINKAGE; Y CHROMOSOME; EVALUATION; FETUS DISEASE; GENETIC MARKER; GENETICS; METHODOLOGY; NOONAN SYNDROME;

ANEUPLOIDY; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 21; FEMALE; FETAL DISEASES; GENETIC MARKERS; HUMANS; MALE; NOONAN SYNDROME; POLYMERASE CHAIN REACTION; TANDEM REPEAT SEQUENCES; TURNER SYNDROME; X CHROMOSOME; Y CHROMOSOME;

EID: 0034747480     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1469-1809.2001.6550421.x     Document Type: Article

References (16)

1. Detection of fetal cells in transcervical samples using X22
2. Rapid detection of aneuploidies by microsatellite and the quantitative fluorescent polymerase chain reaction
3. Prenatal screening of aneuploidies by quantitative fluorescent PCR
4. Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: Experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial
5. Rapid detection of chromosomes X and Y aneuploidies by quantitative fluorescent PCR
6. False-negative finding in rapid interphase FISH analysis of uncultured amniotic cells
7. A prospective comparative study on fluorescence in situ hybridisation (FISH) of uncultured amniocytes and standard karyotype analysis
8. Diagnosis of Down syndrome and other aneuploidies using quantitative polymerase chain reaction and small tandem repeat polymorphisms
9. Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: First application on 247 chorionic villus samples
10. Rapid prenatal diagnosis of aneuploidy by quantitative fluorescent PCR on fetal samples from mothers at high risk for chromosome disorders
11. Quantitative fluorescence polymerase chain reaction for the rapid prenatal detection of common aneuploidies and fetal sex
12. Rapid detection of trisomies 21 and 18 and sexing by quantitative fluorescent multiplex PCR
13. Assessment of diagnostic quantitative fluorescent multiplex polymerase chain reaction assays performed on single cells
14. Detection of aneuploidy in chromosomes X, Y, 13, 18 and 21 by QF-PCR in 662 selected pregnancies at risk
15. A rapid and quantitative DNA sex test: Fluorescence-based PCR analysis of X-Y homologous gene amelogenin
16. Rapid and simple prenatal DNA diagnosis of Down's syndrome