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H F Busch

Showing results (61-70 of 63) with videos related to

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Neurology|January 27, 1998
A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesI F de Coo, E A Sistermans, I J de Wijs, et al.
Journal of Neurology|September 19, 2000
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophyH B Ginjaar, A J van der Kooi, H Ceelie, et al.
Brain : a Journal of Neurology|October 1, 1996
The clinical spectrum of limb girdle muscular dystrophy. A survey in The NetherlandsA J van der Kooi, P G Barth, H F Busch, et al.
Pageof 7

Showing results (61-70 of 63) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 63 results.
Neurology|January 27, 1998
A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesI F de Coo, E A Sistermans, I J de Wijs, et al.
Journal of Neurology|September 19, 2000
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophyH B Ginjaar, A J van der Kooi, H Ceelie, et al.
Brain : a Journal of Neurology|October 1, 1996
The clinical spectrum of limb girdle muscular dystrophy. A survey in The NetherlandsA J van der Kooi, P G Barth, H F Busch, et al.
Pageof 7