Screening auf Fehlbildungen und Chromosomenstörungen

Author:

Zimmermann R.

Publisher

Springer Berlin Heidelberg

Reference31 articles.

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2. Brock DJH (1992) Alphafetoprotein and acetylcholinesterase. In: Brock DJH, Rodeck CH, Ferguson-Smith MA (eds) Prenatal diagnosis and screening. Churchill Livingstone, Edinburgh, pp 159–168

3. Chitty LS (1995) Ultrasonound screening for fetal abnormalities. Prenat Diagn 15: 1241–1257

4. Cicero S, Curcio P, Papageorghiou A, Sonek J, Nicolaides K (2001) Absence of nasal bone in fetuses with trisomy 21 at 11—14 weeks of gestation: an observational study. Lancet 358: 1665–1667

5. Cuckle HS, Wald NJ (1993) Complementary use of biochemical tests and ultrasonography for detection of neural tube defects and Down’s syndrome: Diagnosis. In: Chervenak FA, Isaacson GC, Campbell S (eds) Ultrasound in obstetrics and gynecology. Little, Brown, Boston, pp 1145–1150

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