|
Volumn 47, Issue 11, 2012, Pages 808-812
|
[Value of detection of cell-free fetal DNA in maternal plasma in the prenatal diagnosis of chromosomal abnormalities].
|
Author keywords
[No Author keywords available]
|
Indexed keywords
DNA;
ADULT;
AMNIOCENTESIS;
ANEUPLOIDY;
BLOOD;
CHROMOSOME 18;
CHROMOSOME 21;
CHROMOSOME ABERRATION;
DOWN SYNDROME;
FEMALE;
FOLLOW UP;
GENETICS;
GESTATIONAL AGE;
HUMAN;
KARYOTYPING;
MATERNAL AGE;
MATERNAL SERUM SCREENING TEST;
PREGNANCY;
PRENATAL DIAGNOSIS;
PROCEDURES;
SENSITIVITY AND SPECIFICITY;
TRISOMY;
ADULT;
AMNIOCENTESIS;
ANEUPLOIDY;
CHROMOSOME ABERRATIONS;
CHROMOSOMES, HUMAN, PAIR 18;
CHROMOSOMES, HUMAN, PAIR 21;
DNA;
DOWN SYNDROME;
FEMALE;
FOLLOW-UP STUDIES;
GESTATIONAL AGE;
HUMANS;
KARYOTYPING;
MATERNAL AGE;
MATERNAL SERUM SCREENING TESTS;
PREGNANCY;
PRENATAL DIAGNOSIS;
SENSITIVITY AND SPECIFICITY;
TRISOMY;
|
EID: 84891407599
PISSN: 0529567X
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (5)
|
References (0)
|