Current status of testing for microdeletion syndromes and rare autosomal trisomies using cell-free DNA technology

Obstetrics and Gynecology

Volumn 126, Issue 5, 2015, Pages 1095-1099

  Yaron, Yuval ^a   Jani, Jacques ^a   Schmid, Maximilian ^a   Oepkes, Dick ^a  

^a TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

CELL FREE DNA; DNA; UNCLASSIFIED DRUG;

AUTOSOMAL DISORDER; CAT CRY SYNDROME; CHROMOSOME DELETION; CHROMOSOME DELETION 22Q11; DIAGNOSTIC ACCURACY; DIGEORGE SYNDROME; DNA DETERMINATION; GENETIC PROCEDURES; HAPPY PUPPET SYNDROME; HIGH RISK POPULATION; HUMAN; INVASIVE PROCEDURE; MATERNAL PLASMA; MICROARRAY ANALYSIS; MONOSOMY; MONOSOMY 1P36; NON INVASIVE PROCEDURE; PRADER WILLI SYNDROME; PREDICTIVE VALUE; PREGNANCY; PRENATAL DIAGNOSIS; PRENATAL SCREENING; PRIORITY JOURNAL; RARE DISEASE; REVIEW; TRIPLOIDY; TRISOMY; TRISOMY 13; TRISOMY 16; TRISOMY 21; TRISOMY 22; TRISOMY 9; CHROMOSOME 22; FEMALE; MATERNAL SERUM SCREENING TEST;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; MATERNAL SERUM SCREENING TESTS; PREDICTIVE VALUE OF TESTS; PREGNANCY; TRISOMY;

EID: 84945119197     PISSN: 00297844     EISSN: 1873233X     Source Type: Journal    
DOI: 10.1097/AOG.0000000000001091     Document Type: Review

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