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M M Davidson

Showing results (41-50 of 45) with videos related to

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European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|September 11, 1999
Evidence-based diagnosis of Lyme diseaseM M Davidson, C L Ling, S M Chisholm, et al.
The American Journal of Surgical Pathology|September 8, 2000
Primary cutaneous B-cell lymphoma and Borrelia burgdorferi infection in patients from the Highlands of ScotlandJ R Goodlad, M M Davidson, K Hollowood, et al.
Neurology|September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNAC L Karadimas, P Greenstein, C M Sue, et al.
Communications in Agricultural and Applied Biological Sciences|April 25, 2006
Evaluation of transgenic approaches for controlling tuber moth in potatoesS Meiyalaghan, M F G Takla, O Jaimess, et al.
Nature Genetics|November 5, 1999
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly geneL C Papadopoulou, C M Sue, M M Davidson, et al.
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Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|September 11, 1999
Evidence-based diagnosis of Lyme diseaseM M Davidson, C L Ling, S M Chisholm, et al.
The American Journal of Surgical Pathology|September 8, 2000
Primary cutaneous B-cell lymphoma and Borrelia burgdorferi infection in patients from the Highlands of ScotlandJ R Goodlad, M M Davidson, K Hollowood, et al.
Neurology|September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNAC L Karadimas, P Greenstein, C M Sue, et al.
Communications in Agricultural and Applied Biological Sciences|April 25, 2006
Evaluation of transgenic approaches for controlling tuber moth in potatoesS Meiyalaghan, M F G Takla, O Jaimess, et al.
Nature Genetics|November 5, 1999
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly geneL C Papadopoulou, C M Sue, M M Davidson, et al.
Pageof 5