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Genetic Epidemiology|December 22, 1999
Analyses of the COGA data set in one ethnic group with examinations of alternative definitions of alcoholismL J Sheffield, M P Knauert, A J Pakstis, et al.
Prenatal Diagnosis|May 1, 1995
New estimates of Down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined populationJ L Halliday, L F Watson, J Lumley, et al.
Frontiers in Psychiatry|September 7, 2021
Quantifying the Impact of Phenoconversion on Medications With Actionable Pharmacogenomic Guideline Recommendations in an Acute Aged Persons Mental Health SettingSam Mostafa, Thomas M Polasek, Leslie J Sheffield, et al.
The Journal of Experimental Medicine|October 1, 1985
Direct evidence that a class II molecule and a simple globular protein generate multiple determinantsP M Allen, D J McKean, B N Beck, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Learning-Dependent Shift from Right to Left CA3 Input Dominance Shapes the Evolution of Right CA1 Spatial MapsAnqi Jiang, Douglas GoodSmith, Julliana Ramirez-Matias, et al.
Antimicrobial Agents and Chemotherapy|February 1, 1990
In vitro activities of tosufloxacin, temafloxacin, and A-56620 against pathogens of diarrheaJ P Bryan, C Waters, J Sheffield, et al.
Protein Expression and Purification|April 3, 2001
Expression, purification, and crystallization of the RGS-like domain from the Rho nucleotide exchange factor, PDZ-RhoGEF, using the surface entropy reduction approachS M Garrard, K L Longenecker, M E Lewis, et al.
The British Journal of Surgery|March 30, 2004
Tumour morphology as a predictor of outcome after local excision of rectal cancerW M Chambers, U Khan, A Gagliano, et al.
Australian Dental Journal|December 1, 1992
Binder's syndrome due to prenatal vitamin K deficiency: a theory of pathogenesisA M Howe, W S Webster, A H Lipson, et al.
Molecular Genetics and Metabolism|December 23, 1999
Late diagnosis of maternal PKU in a family segregating an arylsulfatase [corrected] E mutation causing symmetrical chondrodysplasia punctataH H Dahl, A H Osborn, W M Hutchison, et al.
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