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Volumn 212, Issue 4, 2015, Pages 548-549
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Noninvasive prenatal testing: The importance of pretest trisomy risk and posttest predictive values
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Author keywords
[No Author keywords available]
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Indexed keywords
ANEUPLOIDY;
COUNSELING;
GENETIC COUNSELING;
HUMAN;
LETTER;
MATERNAL AGE;
MATERNAL BLOOD;
MATERNAL SERUM;
PRACTICE GUIDELINE;
PREDICTIVE VALUE;
PRENATAL DIAGNOSIS;
PRENATAL SCREENING;
PREVALENCE;
PRIORITY JOURNAL;
TRISOMY;
TRISOMY 13;
TRISOMY 18;
TRISOMY 21;
CHROMOSOME 13;
CHROMOSOME 18;
CHROMOSOME DISORDERS;
DOWN SYNDROME;
EVALUATION STUDY;
FEMALE;
GENETIC SCREENING;
LABORATORY DIAGNOSIS;
MATERNAL SERUM SCREENING TEST;
PREGNANCY;
RISK ASSESSMENT;
RISK FACTOR;
CHROMOSOME DISORDERS;
CHROMOSOMES, HUMAN, PAIR 13;
CHROMOSOMES, HUMAN, PAIR 18;
DOWN SYNDROME;
FALSE POSITIVE REACTIONS;
FEMALE;
GENETIC TESTING;
HUMANS;
MATERNAL SERUM SCREENING TESTS;
PREDICTIVE VALUE OF TESTS;
PREGNANCY;
RISK ASSESSMENT;
RISK FACTORS;
TRISOMY;
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EID: 84930414024
PISSN: 00029378
EISSN: 10976868
Source Type: Journal
DOI: 10.1016/j.ajog.2014.12.033 Document Type: Letter |
Times cited : (14)
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References (5)
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