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K Donner

Showing results (61-70 of 67) with videos related to

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The Journal of Urology|April 1, 1981
Urodynamics in children. Part II. The pseudoneurogenic bladderM K Hanna, W Di Scipio, K K Suh, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 8, 2023
A novel SERPINA12 variant and first European patients with diffuse palmoplantar keratodermaE Brandt, L Harjama, O Elomaa, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
Refined localisation of the genes for nebulin and titin on chromosome 2q allows the assignment of nebulin as a candidate gene for autosomal recessive nemaline myopathyK Pelin, M Ridanpää, K Donner, et al.
Neuromuscular Disorders : NMD|March 21, 2001
Nebulin expression in patients with nemaline myopathyJ Gurgel-Giannetti, U Reed, M L Bang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathyC Wallgren-Pettersson, K Pelin, P Hilpelä, et al.
Nature Genetics|October 3, 1999
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
The Journal of Urology|April 1, 1981
Urodynamics in children. Part II. The pseudoneurogenic bladderM K Hanna, W Di Scipio, K K Suh, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 8, 2023
A novel SERPINA12 variant and first European patients with diffuse palmoplantar keratodermaE Brandt, L Harjama, O Elomaa, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
Refined localisation of the genes for nebulin and titin on chromosome 2q allows the assignment of nebulin as a candidate gene for autosomal recessive nemaline myopathyK Pelin, M Ridanpää, K Donner, et al.
Neuromuscular Disorders : NMD|March 21, 2001
Nebulin expression in patients with nemaline myopathyJ Gurgel-Giannetti, U Reed, M L Bang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathyC Wallgren-Pettersson, K Pelin, P Hilpelä, et al.
Nature Genetics|October 3, 1999
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.
Pageof 7