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Collagen type VI gene expression in the skin of trisomy 21 fetuses.
von Kaisenberg CS, Brand-Saberi B, Christ B, Vallian S, Farzaneh F, Nicolaides KH.
Obstet Gynecol 1998;91:319-23. -
Defects and syndromes in chromosomally normal fetuses with increased nuchal translucency thickness at 10-14 weeks of gestation.
Souka AP, Snijders RJ, Novakov A, Soares W, Nicolaides KH.
Ultrasound Obstet Gynecol 1998;11:391-400. -
UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10-14 weeks of gestation.
Snijders RJ, Noble P, Sebire N, Souka A, Nicolaides KH.
Lancet 1998;352:343-6. -
Detection of sex chromosome abnormalities by nuchal translucency screening at 10-14 weeks.
Sebire NJ, Snijders RJ, Brown R, Southall T, Nicolaides KH.
Prenat Diagn 1998;18:581-4. -
Personal coping resources, responsibility, anxiety and depression after early pregnancy loss.
Nikcevic AV, Kuczmierczyk AR, Nicolaides KH.
J Psychosom Obstet Gynaecol 1998;19:145-54. -
Psychological outcomes following missed abortions and provision of follow-up care.
Nikcevic AV, Tunkel SA, Nicolaides KH.
Ultrasound Obstet Gynecol 1998;11:123-8. -
Correct estimation of parameters for ultrasound nuchal translucency screening.
Nicolaides KH, Snijders RJ, Cuckle HS.
Prenat Diagn 1998;18:519-23. -
Screening for chromosomal abnormalities at 10-14 weeks: the role of ductus venosus blood flow.
Matias A, Gomes C, Flack N, Montenegro N, Nicolaides KH.
Ultrasound Obstet Gynecol 1998;12:380-4. -
Biochemical analyses of mesenchymal fluid in early pregnancy.
Jauniaux E, Gulbis B, Hyett J, Nicolaides KH.
Am J Obstet Gynecol 1998;178:765-9. -
The umbilical artery pulsatility index in the first trimester: is there an association with increased nuchal translucency or chromosomal abnormality?
Brown R, Di Luzio L, Gomes C, Nicolaides KH.
Ultrasound Obstet Gynecol 1998;12:244-7. -
Outcome of chromosomally normal livebirths with increased fetal nuchal translucency at 10-14 weeks' gestation.
Brady AF, Pandya PP, Yuksel B, Greenough A, Patton MA, Nicolaides KH.
J Med Genet 1998;35:222-4.