Non-invasive prenatal testing for sex chromosome abnormalities: A source of confusion

BMJ Case Reports

Volumn 2015, Issue , 2015, Pages

  Kalafat, Erkan ^a   Seval, Mehmet Murat ^a   Turgay, Batuhan ^a   Koç, Acar ^a  

^a ANKARA UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; AMNION FLUID; AORTA COARCTATION; ARTICLE; CASE REPORT; CELL CULTURE; CELL FREE FETAL DNA TESTING; CHROMOSOME ABERRATION; CHROMOSOME CULTURE; CONFUSION; DIAGNOSIS; FEMALE; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GENETIC SCREENING; GENETICS; GESTATIONAL AGE; HUMAN; INFERTILITY; INTRACYTOPLASMIC SPERM INJECTION; KIDNEY CYST; LABORATORY DIAGNOSIS; LYMPHEDEMA; MATERNAL AGE; MONOSOMY X; NON INVASIVE PRENATAL TESTING; NON INVASIVE PROCEDURE; OBSTETRICS; PREDICTIVE VALUE; PREGNANCY; PRENATAL CARE; PRENATAL DIAGNOSIS; PROCEDURES; SEX CHROMOSOME ABERRATION; SINGLE NUCLEOTIDE POLYMORPHISM; STRUCTURE ANALYSIS; TREATMENT OUTCOME; TURNER SYNDROME;

ADULT; AMNIOCENTESIS; CHROMOSOME ABERRATIONS; DIAGNOSIS; FALSE POSITIVE REACTIONS; FEMALE; GENETIC TESTING; GENETICS; HUMANS; METHODS; PREDICTIVE VALUE OF TESTS; PREGNANCY; PRENATAL DIAGNOSIS; TURNER SYNDROME; ULTRASONOGRAPHY, PRENATAL;

EID: 84964311229     PISSN: None     EISSN: 1757790X     Source Type: Journal    
DOI: 10.1136/bcr-2014-207309     Document Type: Article

References (15)

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