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Volumn 33, Issue 7, 2011, Pages 736-750

Prenatal Screening for Fetal Aneuploidy in Singleton Pregnancies

Author keywords

Aneuploidy; Down syndrome; Genetic health risk; Genetic health surveillance; Prenatal diagnosis; Prenatal screening; Trisomy

Indexed keywords

ANEUPLOIDY; ARTICLE; BIOCHEMISTRY; BIOMEDICAL TECHNOLOGY ASSESSMENT; BLOOD ANALYSIS; CANADA; CHROMOSOME ABERRATION; CHROMOSOME REARRANGEMENT; CONSENSUS DEVELOPMENT; CYTOGENETICS; DISEASE SURVEILLANCE; DOWN SYNDROME; FERTILIZATION IN VITRO; FETUS DISEASE; FETUS ECHOGRAPHY; FIRST TRIMESTER PREGNANCY; GENETIC COUNSELING; GENETIC RISK; GENETIC SCREENING; GYNECOLOGIST; HUMAN; INTRACYTOPLASMIC SPERM INJECTION; INVASIVE PROCEDURE; MATERNAL AGE; NON INVASIVE PROCEDURE; NUCHAL TRANSLUCENCY MEASUREMENT; OBSERVATIONAL STUDY; OBSTETRICIAN; PRACTICE GUIDELINE; PRENATAL SCREENING; RANDOMIZED CONTROLLED TRIAL (TOPIC); RISK ASSESSMENT; SECOND TRIMESTER PREGNANCY; SYSTEMATIC REVIEW (TOPIC); TRISOMY; TRISOMY 13; TRISOMY 18; TRISOMY 21; ADULT; BLOOD; CHROMOSOME 18; FEMALE; GESTATIONAL AGE; LITERATURE; METHODOLOGY; PREGNANCY; PRENATAL DIAGNOSIS; RISK FACTOR;

EID: 82355181830     PISSN: 17012163     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1701-2163(16)34961-1     Document Type: Article
Times cited : (107)

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