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B Estournet-Mathiaud

Showing results (11-20 of 14) with videos related to

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American Journal of Medical Genetics|December 10, 1999
Jeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acidP Labrune, M Fabre, P Trioche, et al.
Neurology|October 10, 2001
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular studyY He, K J Jones, N Vignier, et al.
Neuromuscular Disorders : NMD|October 6, 2005
134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The NetherlandsE Bertini, A Burghes, K Bushby, et al.
European Journal of Neurology|October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
American Journal of Medical Genetics|December 10, 1999
Jeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acidP Labrune, M Fabre, P Trioche, et al.
Neurology|October 10, 2001
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular studyY He, K J Jones, N Vignier, et al.
Neuromuscular Disorders : NMD|October 6, 2005
134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The NetherlandsE Bertini, A Burghes, K Bushby, et al.
European Journal of Neurology|October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Pageof 2