Integrated ultrasound and biochemical screening for trisomy 21 using fetal nuchal translucency, absent fetal nasal bone, free ?-hCG and PAPP-A at 11 to 14 weeks-Reference-Cited by-同舟云学术

Integrated ultrasound and biochemical screening for trisomy 21 using fetal nuchal translucency, absent fetal nasal bone, free ?-hCG and PAPP-A at 11 to 14 weeks

Published:2003 Issue:4 Volume:23 Page:306-310
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Cicero Simona,Bindra Renu,Rembouskos Georgios,Spencer Kevin,Nicolaides Kypros H.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference17 articles.

1. One-stop clinic for assessment of risk for trisomy 21 at 11-14 weeks: a prospective study of 15 030 pregnancies

2. 1991. Ultrasound and biochemical assessment of first trimester pregnancy. In The Embryo: Normal and Abnormal Development and Growth, (eds). Springer-Verlag: New York; 181-194.

3. Absence of nasal bone in fetuses with trisomy 21 at 11–14 weeks of gestation: an observational study

4. REFINEMENTS IN MANAGING MATERNAL WEIGHT ADJUSTMENT FOR INTERPRETING PRENATAL SCREENING RESULTS

5. Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy.

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