Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies

Ultrasound in Obstetrics and Gynecology

Volumn 47, Issue 1, 2016, Pages 53-57

  Li, R ^a   Wan, J ^a   Zhang, Y ^a   Fu, F ^a   Ou, Y ^a   Jing, X ^a   Li, J ^a   Li, D ^a   Liao, C ^a  

^a GUANGZHOU MEDICAL UNIVERSITY   (China)

Author keywords

chromosome deletion; chromosome duplication; chromosome structural abnormality; copy number variations; fetal fraction; non invasive prenatal testing

Indexed keywords

DNA;

ADULT; AMNIOCENTESIS; ANEUPLOIDY; BLOOD; CHORION VILLUS SAMPLING; CHROMOSOME DISORDERS; COPY NUMBER VARIATION; CORDOCENTESIS; DNA SEQUENCE; FEMALE; GENETICS; HUMAN; MICROARRAY ANALYSIS; PREGNANCY; RETROSPECTIVE STUDY; SECOND TRIMESTER PREGNANCY; YOUNG ADULT;

ADULT; AMNIOCENTESIS; ANEUPLOIDY; CHORIONIC VILLI SAMPLING; CHROMOSOME DISORDERS; CORDOCENTESIS; DNA; DNA COPY NUMBER VARIATIONS; FEMALE; HUMANS; MICROARRAY ANALYSIS; PREGNANCY; PREGNANCY TRIMESTER, SECOND; RETROSPECTIVE STUDIES; SEQUENCE ANALYSIS, DNA; YOUNG ADULT;

EID: 84953374210     PISSN: 09607692     EISSN: 14690705     Source Type: Journal    
DOI: 10.1002/uog.14911     Document Type: Article

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