Literatur
- 1
Queisser-Luft A, Stopfkuchen H, Stolz G, Schlaefer K, Merz E.
Prenatal diagnosis of major malformations: Quality control of routine ultrasound examinations
based on a five-year study of 20 248 newborn fetuses and infants.
Prenat Diagn.
1998;
18
567-576
- 2 Snijders R JM, Nicolaides K H. Ultrasound markers for fetal chromosomal defects. New
York - London; Parthenon 1996
- 3
Conde-Agudelo A, Kafury-Goeta A C.
Triple-marker test as screening for Down syndrome: a meta-analysis.
Obstet Gynecol Surv.
1998;
53
369-376
- 4
Bernaschek G, Kolankaya A, Stuepflen I, Deutinger J.
Chromosomal abnormalities: how much can we predict by ultrasound examination in low-risk
pegnancies?.
Am J Perinatol.
1996;
13
259-263
- 5
Smith-Bindman R, Hosmer W, Feldstein V A, Deeks J J, Goldberg J D.
Second-trimester ultrasound to detect fetuses with Down syndrome. A meta-analysis.
JAMA.
2001;
285
1044-1055
- 6 Nicolaides K H, Sebire N J, Snijders R JM. The 11 - 14 week scan - Diagnosis of
fetal abnormalities. New York, London; Parthenon Publishing 1999
- 7
PAPP-A .
Ultrasound.
Obstet Gynecol.
1999;
13
231-237
- 8
Snijders R JM, Noble P, Sebire N, Souka A, Nicolaides K H.
UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal
nuchal translucency thickness at 10 - 14 weeks of gestation.
Lancet.
1998;
351
343-346
- 9
Nicolaides K H, Cicero S, Liao A W.
One stop clinic for assessment of risk of chromosomal defects at 12 weeks of gestation.
Prenat Neonat Med.
2000;
5
145- 154
E. Merz
Gynäkologie und Geburthilfe · Krankenhaus Nordwest
Frankfurt/Main
