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Cerebellar hypoplasia, facial dysmorphism and internal abnormalities: a new recessive syndrome?
Seller MJ, Pal K, Moscoso G, Nicolaides K, Hyett JA.
Clin Dysmorphol 1998;7:41-4. -
Audit of prenatal diagnosis for hemoglobin disorders in the United Kingdom The first twenty years.
Modell B, Petrou M, Layton M, Varnavides L, Moisely C, Ward RH, Rodeck C, Nicolaides K, Fitches A, Old J.
Ann N Y Acad Sci 1998;850:420-2. -
Diagnosis of the Meckel-Gruber syndrome at eleven to fourteen weeks gestation.
Sepulveda W, Sebire NJ, Souka A, Snijders RJ, Nicolaides KH.
Am J Obstet Gynecol 1997;176:316-9. -
Audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: The first 20 years.
Modell B, Petrou M, Layton M, Varnavides L, Slater C, Ward R H, Rodeck C, Nicolaides KH, Gibbons S, Fitches A, Old J.
BMJ 1997;315:779-84. -
Ultrasound screening for anencephaly at 10-14 of gestation.
Johnson SP, Sebire NJ, Snijders RJM, Tunkel S, Nicolaides KH.
Ultrasound Obstet Gynecol 1997;9:14-6. -
Lethal congenital arthrogryposis presents with increased nuchal translucency at 10-14 weeks of gestation.
Hyett JH, Noble P, Sebire NJ, Snijders RJM, Nicolaides KH.
Ultrasound Obstet Gynecol 1997;9:310-3. -
Superovulation, IGFBP-1 and birth weight.
Johnson MR, Irvine R, Hills F, Bolton VN, Abbas AA, Brooks AA, Allman AC, Chard T, Nicolaides KH.
Eur J Obstet Gynecol Reprod Biol 1995;59:193-5. -
Increased first trimester nuchal translucency as a prenatal manifestation of Smith-Lemli-Opitz syndrome.
Hyett JA, Clayton PT, Moscoso G, Nicolaides KH.
Am J Med Genet 1995;58:374-6.