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Volumn 211, Issue 6, 2014, Pages 711-712
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Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA
a b c |
Author keywords
[No Author keywords available]
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Indexed keywords
GENOMIC DNA;
AMNION FLUID ANALYSIS;
CELL FREE SYSTEM;
CHORION VILLUS SAMPLING;
CHROMOSOME ANALYSIS;
CYTOTROPHOBLAST;
DNA SEQUENCE;
FALSE POSITIVE RESULT;
FEMALE;
HUMAN;
KARYOTYPING;
LETTER;
MATERNAL BLOOD;
MOSAICISM;
NON INVASIVE PROCEDURE;
NONINVASIVE PRENATAL SCREENING;
PRENATAL SCREENING;
PRIORITY JOURNAL;
SENSITIVITY AND SPECIFICITY;
SEX CHROMOSOME ABERRATION;
TRISOMY 13;
TRISOMY 18;
TRISOMY 21;
TROPHOBLAST;
GENOMICS;
HIGH THROUGHPUT SEQUENCING;
MATERNAL SERUM SCREENING TEST;
PREGNANCY;
PROCEDURES;
SEX CHROMOSOME DISORDERS;
TRISOMY;
FEMALE;
GENOMICS;
HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING;
HUMANS;
MATERNAL SERUM SCREENING TESTS;
PREGNANCY;
SEQUENCE ANALYSIS, DNA;
SEX CHROMOSOME ABERRATIONS;
SEX CHROMOSOME DISORDERS;
TRISOMY;
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EID: 84922522575
PISSN: 00029378
EISSN: 10976868
Source Type: Journal
DOI: 10.1016/j.ajog.2014.07.015 Document Type: Letter |
Times cited : (14)
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References (4)
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