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Human Mutation|May 25, 1999
Genetic diagnosis of 21-hydroxylase deficiency: DGGE-based mutation scanning of CYP21G Ohlsson, J Müller, M Schwartz
Health Care Financing Review|December 4, 1993
An evaluation of pediatric-modified diagnosis-related groupsS M Payne, R M Schwartz
Memory (Hove, England)|January 6, 2001
The impersistence of false memory persistenceJ M Lampinen, R M Schwartz
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|June 1, 1995
Cell death suffers a TKOB A Osborne, L M Schwartz
Prenatal Diagnosis|February 1, 1996
First-trimester prenatal diagnosis of Crouzon syndromeM Schwartz, S Kreiborg, F Skovby
The Journal of Laboratory and Clinical Medicine|February 1, 1993
Comparison of glomerular injury in juvenile versus mature rats in a remnant kidney modelM M Schwartz, A K Bidani
Paediatric and Perinatal Epidemiology|January 1, 1997
Risk of recurrence of birth defects in Washington StateB A Mueller, S M Schwartz
In Vitro|May 1, 1983
Technique for cloning bovine aortic endothelial cellsC M Gajdusek, S M Schwartz
In Vitro|October 1, 1984
Effect of clonal senescence on low density lipoprotein-receptor activity of bovine arterial endothelial cellsE L Bierman, S M Schwartz
Journal of Cellular Physiology|January 1, 1982
Ability of endothelial cells to condition culture mediumC M Gajdusek, S M Schwartz
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