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Volumn 107, Issue 2, 2000, Pages 262-266
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Effectiveness of prenatal chromosomal analysis using multicolour fluorescent in situ hybridisation
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Author keywords
[No Author keywords available]
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Indexed keywords
SATELLITE DNA;
AMNION FLUID;
ANEUPLOIDY;
ARTICLE;
CENTROMERE;
CHROMOSOME 13;
CHROMOSOME 18;
CHROMOSOME 21;
CHROMOSOME ABERRATION;
CHROMOSOME ANALYSIS;
CLINICAL TRIAL;
CONGENITAL DISORDER;
CONTROLLED CLINICAL TRIAL;
CONTROLLED STUDY;
DEVICE;
DIAGNOSTIC ACCURACY;
DNA PROBE;
FEMALE;
FETUS;
FETUS ECHOGRAPHY;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENETIC SCREENING;
HUMAN;
HUMAN CELL;
MAJOR CLINICAL STUDY;
MALE;
OUTCOMES RESEARCH;
PHENOTYPE;
PRENATAL DIAGNOSIS;
PRIORITY JOURNAL;
PROSPECTIVE STUDY;
TIME;
TRISOMY;
X CHROMOSOME;
Y CHROMOSOME;
CHROMOSOME ABERRATIONS;
CHROMOSOME DISORDERS;
COLOR;
FEMALE;
GENETIC SCREENING;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
MALE;
PREGNANCY;
PRENATAL DIAGNOSIS;
PROSPECTIVE STUDIES;
SENSITIVITY AND SPECIFICITY;
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EID: 0033983677
PISSN: 14700328
EISSN: 14710528
Source Type: Journal
DOI: 10.1111/j.1471-0528.2000.tb11698.x Document Type: Article |
Times cited : (42)
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References (7)
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