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B Wirth

Showing results (111-120 of 119) with videos related to

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Annals of Neurology|October 23, 1997
Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy regionR Korinthenberg, M Sauer, U P Ketelsen, et al.
Human Genetics|September 10, 1999
Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminomaF von Deimling, J M Scharf, T Liehr, et al.
Genomics|May 1, 1992
The gene for autosomal dominant polycystic kidney disease lies in a 750-kb CpG-rich regionG G Germino, D Weinstat-Saslow, H Himmelbauer, et al.
Neurology|March 26, 2003
Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathyS Rudnik-Schöneborn, H H Goebel, W Schlote, et al.
Genomics|April 1, 1988
Two different genes for X-linked retinitis pigmentosaB Wirth, M J Denton, J D Chen, et al.
Der Urologe. Ausg. A|December 26, 2015
[Prostate biopsy: Procedure in the clinical routine]T Enzmann, T Tokas, K Korte, et al.
American Journal of Human Genetics|October 16, 1999
Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21K Grohmann, T F Wienker, K Saar, 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.
Brain Research Bulletin|August 24, 2010
Development of quantitative and sensitive assessments of physiological and functional outcome during recovery from spinal cord injury: a clinical initiativeP H Ellaway, A Kuppuswamy, A V Balasubramaniam, et al.
Pageof 12

Showing results (111-120 of 119) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 119 results.
Annals of Neurology|October 23, 1997
Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy regionR Korinthenberg, M Sauer, U P Ketelsen, et al.
Human Genetics|September 10, 1999
Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminomaF von Deimling, J M Scharf, T Liehr, et al.
Genomics|May 1, 1992
The gene for autosomal dominant polycystic kidney disease lies in a 750-kb CpG-rich regionG G Germino, D Weinstat-Saslow, H Himmelbauer, et al.
Neurology|March 26, 2003
Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathyS Rudnik-Schöneborn, H H Goebel, W Schlote, et al.
Genomics|April 1, 1988
Two different genes for X-linked retinitis pigmentosaB Wirth, M J Denton, J D Chen, et al.
Der Urologe. Ausg. A|December 26, 2015
[Prostate biopsy: Procedure in the clinical routine]T Enzmann, T Tokas, K Korte, et al.
American Journal of Human Genetics|October 16, 1999
Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21K Grohmann, T F Wienker, K Saar, 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.
Brain Research Bulletin|August 24, 2010
Development of quantitative and sensitive assessments of physiological and functional outcome during recovery from spinal cord injury: a clinical initiativeP H Ellaway, A Kuppuswamy, A V Balasubramaniam, et al.
Pageof 12