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Volumn 16, Issue 8, 2016, Pages 759-766

Clinical experience of non-invasive prenatal chromosomal aneuploidy testing in 190,277 patient samples

Author keywords

Clinical experience; Copy number variation (CNVs); False negative; Mosaicism; Noninvasive prenatal testing (NIPT); Trisomy

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; COPY NUMBER VARIATION; DNA LIBRARY; FEMALE; GENE SEQUENCE; GESTATIONAL AGE; HUMAN; HUMAN TISSUE; KARYOTYPING; MATERNAL SERUM SCREENING TEST; POLYMERASE CHAIN REACTION; PREDICTIVE VALUE; PRENATAL SCREENING; SEMICONDUCTOR SEQUENCING; SENSITIVITY AND SPECIFICITY; SEX CHROMOSOME; SPONTANEOUS ABORTION; TRISOMY 13; TRISOMY 18; TRISOMY 21; ADOLESCENT; CLINICAL TRIAL; DOWN SYNDROME; HEALTH SURVEY; MIDDLE AGED; MOSAICISM; MULTICENTER STUDY; PREGNANCY; PRENATAL DIAGNOSIS; REPRODUCIBILITY; TRISOMY; YOUNG ADULT;

EID: 84995961254     PISSN: 15665240     EISSN: 18755666     Source Type: Journal    
DOI: 10.2174/1566524016666161013142335     Document Type: Article
Times cited : (39)

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