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Human Molecular Genetics|May 23, 1998
Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxicationE P Treacy, B R Akerman, L M Chow, et al.
Clinical Genetics|February 1, 1982
Three distinct types of X-linked arthrogryposis seen in 6 familiesJ G Hall, S D Reed, C I Scott, et al.
Physics in Medicine and Biology|October 1, 1986
Design of an efficient position sensitive gamma ray detector for nuclear medicineJ G Rogers, D P Saylor, R Harrop, et al.
Transplantation Proceedings|June 27, 2006
Effect of age on outcomes after left ventricular assist device placementR Huang, M Deng, J G Rogers, et al.
Pediatric Radiology|January 1, 1987
Atelosteogenesis: evidence for heterogeneityD O Sillence, K Kozlowski, J G Rogers, et al.
American Journal of Medical Genetics|March 1, 1990
Autosomal recessive hydrocephalus with third ventricle obstructionC W Chow, P A McKelvie, R M Anderson, et al.
The American Journal of Cardiovascular Pathology|January 1, 1989
Myocardial fibrosis in endomyocardial biopsy specimens: do different bioptomes affect estimation?C R Meckel, J E Wilson, T D Sears, et al.
The American Journal of Physiology|March 5, 1998
The human plasminogen activator inhibitor type I gene promoter targets to kidneyM P Emert, C M Sorenson, D P Basile, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 5, 1981
New metabolites in isovaleric acidemiaR J Truscott, D Malegan, E McCairns, et al.
The New England Journal of Medicine|September 16, 1976
Increased nerve-growth-factor beta-chain cross-reacting material in familial dysautonomiaD C Siggers, J G Rogers, S H Boyer, et al.
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