Clinical experience and follow-up with large-scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing

American Journal of Obstetrics and Gynecology

Volumn 213, Issue 2, 2015, Pages 253-

  Singh, Onkar Nath ^a  

^a GREATER BALTIMORE MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; CONGENITAL MALFORMATION; FALSE NEGATIVE RESULT; FALSE POSITIVE RESULT; FOLLOW UP; HIGH RISK POPULATION; HUMAN; LETTER; LOW RISK POPULATION; NON INVASIVE PROCEDURE; PREDICTIVE VALUE; PRENATAL SCREENING; PRIORITY JOURNAL; QUALITY CONTROL; SINGLE NUCLEOTIDE POLYMORPHISM; SPONTANEOUS ABORTION; CHROMOSOME DISORDERS; DOWN SYNDROME; FEMALE; GENETICS; PREGNANCY; TRISOMY; TURNER SYNDROME;

DNA;

CHROMOSOME DISORDERS; DNA; DOWN SYNDROME; FEMALE; HUMANS; PREGNANCY; TRISOMY; TURNER SYNDROME;

EID: 84937977668     PISSN: 00029378     EISSN: 10976868     Source Type: Journal    
DOI: 10.1016/j.ajog.2015.04.039     Document Type: Letter

References (1)

1. P. Dar, K.J. Curnow, S.J. Gross, and et al. Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing Am J Obstet Gynecol 211 2014 527.e1 527.e17