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Volumn 16, Issue 6, 2010, Pages 427-433

Rapid aneuploidy screening with fluorescence in-situ hybridisation: Is it a sufficiently robust stand-alone test for prenatal diagnosis?

Author keywords

Aneuploidy; Fluorescence; In situ hybridization; Karyotyping; Prenatal diagnosis

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME ABERRATION; CHROMOSOME MOSAICISM; CHROMOSOME REARRANGEMENT; CONTROLLED STUDY; DIAGNOSTIC ERROR; DIAGNOSTIC TEST ACCURACY STUDY; ECHOGRAPHY; FALSE NEGATIVE RESULT; FALSE POSITIVE RESULT; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC SCREENING; HUMAN; KARYOTYPE; KARYOTYPE 47,XXX; KARYOTYPE 47,XXY; KARYOTYPE 47,XYY; MAJOR CLINICAL STUDY; MEDICAL RECORD REVIEW; MONOSOMY X; PRENATAL DIAGNOSIS; RETROSPECTIVE STUDY; SENSITIVITY AND SPECIFICITY; SINGAPORE; TRIPLOIDY; TRISOMY 13; TRISOMY 18; TRISOMY 21; UNITED STATES; X CHROMOSOME; Y CHROMOSOME;

EID: 79951496282     PISSN: 10242708     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (7)

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