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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 7, 2022
Change in prevalence of preterm birth in Israel following publication of national guidelines recommending routine sonographic cervical-length measurement at 19-25 weeks' gestationR Maymon, M Pekar-Zlotin, H Meiri, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 15, 2007
Combining fetal nuchal fold thickness with second-trimester biochemistry to screen for trisomy 21A Borrell, I Mercade, E Casals, et al.
Lancet (London, England)|June 25, 1977
Maternal serum-alpha-fetoprotein measurement in antenatal screening for anencephaly and spina bifida in early pregnancy. Report of U.K. collaborative study on alpha-fetoprotein in relation to neural-tube defectsN J Wald, H Cuckle, J H Brock, et al.
British Journal of Obstetrics and Gynaecology|August 1, 1996
Antenatal screening for cystic fibrosisH Cuckle, P Quirke, I Sehmi, et al.
American Journal of Obstetrics and Gynecology|October 1, 1994
Isolated choroid plexus cyst(s): an indication for amniocentesisM J Kupferminc, R K Tamura, R E Sabbagha, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 27, 2025
Whole-genome paternal uniparental disomy identified through prenatal single-nucleotide polymorphism-based cell-free DNA screeningP Benn, K Hashimoto, V Souter, et al.
Prenatal Diagnosis|August 1, 1996
Trisomy 16 mosaicism in amniotic fluid cell culturesU Tantravahi, C Matsumoto, J Delach, et al.
British Journal of Haematology|February 1, 1992
Cytogenetic studies of bone marrow fibroblasts cultured from patients with myelofibrosis and myeloid metaplasiaJ C Wang, H D Lang, S Lichter, et al.
The Journal of Rheumatology|April 1, 1990
Pharmacokinetics of auranofin a single dose study in manH P Benn, C Schnier, K U Seiler, et al.
Leukemia|November 1, 1988
A rare restriction enzyme site polymorphism in the breakpoint cluster region (bcr) of chromosome 22P Benn, A Grossman, L Soper, et al.
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