Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH)

Prenatal Diagnosis

Volumn 22, Issue 1, 2002, Pages 29-33

  Witters, Ingrid ^a,b   Devriendt, K ^a   Legius, E ^a   Matthijs, G ^a   Van Schoubroeck, D ^a   Van Assche, F A ^a   Fryns, Jean Pierre ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Amniocentesis; Chromosome 21; Interphase FISH; Prenatal diagnosis

Indexed keywords

AMNIOCENTESIS; AMNION FLUID ANALYSIS; ANEUPLOIDY; ARTICLE; CHROMOSOME 13; CHROMOSOME 21; CHROMOSOME 8; CHROMOSOME REARRANGEMENT; DOWN SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; HIGH RISK POPULATION; HUMAN; HUMAN CELL; INTERPHASE; KARYOTYPE; MAJOR CLINICAL STUDY; NUMERICAL CHROMOSOME ABERRATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RELIABILITY; RETROSPECTIVE STUDY; ROBERTSONIAN CHROMOSOME TRANSLOCATION; TRISOMY 21; X CHROMOSOME; Y CHROMOSOME;

AMNIOCENTESIS; AMNIOTIC FLUID; ANEUPLOIDY; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 21; CYTOGENETIC ANALYSIS; DOWN SYNDROME; FEMALE; FETAL GROWTH RETARDATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; OLIGOHYDRAMNIOS; PREGNANCY; PRENATAL DIAGNOSIS; SEX CHROMOSOME ABERRATIONS; TRISOMY; ULTRASONOGRAPHY, PRENATAL; X CHROMOSOME; Y CHROMOSOME;

ROBERTSONIA;

EID: 0036173354     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.225     Document Type: Article

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