Non-Invasive Chromosomal Evaluation (NICE) Study: Results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18

American Journal of Obstetrics and Gynecology

Volumn 207, Issue 2, 2012, Pages 137.e1-137.e8

  Norton, Mary E ^a   Brar, Herb ^b   Weiss, Jonathan ^c   Karimi, Ardeshir ^d   Laurent, Louise C ^e   Caughey, Aaron B ^j   Rodriguez, M Hellen ^f   Williams III, John ^g   Mitchell, Michael E ^l   Adair, Charles D ^m   Lee, Hanmin ^h   Jacobsson, Bo ⁿ   Tomlinson, Mark W ^k   Oepkes, Dick ^o   Hollemon, Desiree ⁱ   Sparks, Andrew B ⁱ   Oliphant, Arnold ⁱ   Song, Ken ⁱ  

^a STANFORD UNIVERSITY   (United States)

^b Riverside Perinatal Diagnostic Center   (United States)

^c East Bay Perinatal Medical Associates   (United States)

^d Institute of Prenatal Diagnosis and Reproductive Genetics   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

^f San Gabriel Valley Perinatal Medical Group   (United States)

^g CEDARS SINAI MEDICAL CENTER   (United States)

^h UNIVERSITY OF CALIFORNIA   (United States)

ⁱ Ariosa Diagnostics   (United States)

^j OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^k Northwest Perinatal Center   (United States)

^l MEDICAL COLLEGE OF WISCONSIN   (United States)

^m UNIVERSITY OF TENNESSEE COLLEGE OF MEDICINE   (United States)

ⁿ SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

^o LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

more..

Author keywords

aneuploidy detection; cell free fetal DNA; Down syndrome; noninvasive prenatal diagnosis; trisomy

Indexed keywords

CELL DNA;

ADULT; AMNIOCENTESIS; ANEUPLOIDY; ARTICLE; CELL FREE SYSTEM; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME ANALYSIS; CHROMOSOME SELECTIVE SEQUENCING; CLINICAL STUDY; COHORT ANALYSIS; CONTROLLED STUDY; DIAGNOSTIC TEST ACCURACY STUDY; DNA ISOLATION; DNA SEQUENCE; FALSE POSITIVE RESULT; FEMALE; FETUS; GENETIC ALGORITHM; GENETIC RISK; HUMAN; MAJOR CLINICAL STUDY; MULTICENTER STUDY; MULTICENTER STUDY (TOPIC); NON INVASIVE PROCEDURE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PROSPECTIVE STUDY; RISK ASSESSMENT; SENSITIVITY AND SPECIFICITY; TRISOMY 18; TRISOMY 21;

EID: 84864408781     PISSN: 00029378     EISSN: 10976868     Source Type: Journal    
DOI: 10.1016/j.ajog.2012.05.021     Document Type: Article

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