Showing results (191-200 of 442) with videos related to
Sort By:
Pageof 45
Journal of the American Optometric Association|November 1, 1985
Soft bifocal contact lenses for patients with nearpoint asthenopiaD P Libassi, C L Barron, R LondonPlastic and Reconstructive Surgery. Global Open|May 25, 2026
Scaphotrapeziotrapezoid Fusion for Chemotherapy-induced Capitate Avascular NecrosisJessica J Farzan, Sivana L Barron, Anselm WongJournal of Advanced Nursing|September 1, 1987
An examination of preconception health teaching by nurse practitionersM L Barron, L H Ganong, M BrownClinical Genetics|February 11, 2000
Transcervical cells and the prenatal diagnosis of haemoglobin (Hb) mutationsV Cirigliano, J Sherlock, M Petrou, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancyD S Millar, J Allgrove, C Rodeck, et al.Prenatal Diagnosis|October 8, 1997
Prenatal screening for cystic fibrosis carriers: does the method of testing affect the longer-term understanding and reproductive behaviour of women?M E Mennie, D Axworthy, W A Liston, et al.Human Genetics|September 1, 1988
Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosisL Strain, A Curtis, M Mennie, et al.American Journal of Human Genetics|February 1, 1994
Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3L Strain, C M Gosden, D J Brock, et al.Journal of Reproduction and Fertility|September 1, 1978
Fetal- and uterine-specific antigens in human amniotic fluidR G Sutcliffe, D J Brock, L V Nicholson, et al.Molecular and Cellular Probes|August 1, 1994
Identification of a novel exon 4 SOD1 mutation in a sporadic amyotrophic lateral sclerosis patientC T Jones, P J Shaw, G Chari, et al.Pageof 45