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D J Watts

Showing results (51-60 of 54) with videos related to

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Clinical Genetics|August 23, 2012
Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementiaS G Mehta, M Khare, R Ramani, et al.
American Journal of Medical Genetics. Part A|February 9, 2008
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementiaVirginia E Kimonis, Sarju G Mehta, Erin C Fulchiero, et al.
Journal of Neuropathology and Experimental Neurology|June 20, 2006
Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutationsMark S Forman, Ian R Mackenzie, Nigel J Cairns, et al.
Nature Genetics|September 28, 2005
Mutations in SEPT9 cause hereditary neuralgic amyotrophyGregor Kuhlenbäumer, Mark C Hannibal, Eva Nelis, et al.
Pageof 6

Showing results (51-60 of 54) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 54 results.
Clinical Genetics|August 23, 2012
Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementiaS G Mehta, M Khare, R Ramani, et al.
American Journal of Medical Genetics. Part A|February 9, 2008
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementiaVirginia E Kimonis, Sarju G Mehta, Erin C Fulchiero, et al.
Journal of Neuropathology and Experimental Neurology|June 20, 2006
Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutationsMark S Forman, Ian R Mackenzie, Nigel J Cairns, et al.
Nature Genetics|September 28, 2005
Mutations in SEPT9 cause hereditary neuralgic amyotrophyGregor Kuhlenbäumer, Mark C Hannibal, Eva Nelis, et al.
Pageof 6