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Neurogenetics

Showing results (631-640 of 949) with videos related to

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Neurogenetics|September 21, 2010
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variabilityLucio Santoro, Guido J Breedveld, Fiore Manganelli, et al.
Neurogenetics|February 3, 2009
Examination of association of genes in the serotonin system to autismB M Anderson, N C Schnetz-Boutaud, J Bartlett, et al.
Neurogenetics|April 7, 2010
LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Neurogenetics|May 6, 2010
Myotonic dystrophy type I combined with X-linked dominant Charcot-Marie-Tooth neuropathyHyun Sook Kim, Ki Wha Chung, Sung Hee Kang, et al.
Neurogenetics|September 25, 2009
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 geneGabriele Dekomien, Conni Vollrath, Elisabeth Petrasch-Parwez, et al.
Neurogenetics|October 7, 2006
Complex gene-gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genesAlison A Motsinger, David Brassat, Stacy J Caillier, et al.
Neurogenetics|December 18, 2008
Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)Julien Cassereau, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurogenetics|March 12, 2009
The impact of spermine synthase (SMS) mutations on brain morphologyShelli R Kesler, Charles Schwartz, Roger E Stevenson, et al.
Neurogenetics|June 12, 2009
Reduced levels of survival motor neuron protein leads to aberrant motoneuron growth in a Xenopus model of muscular atrophyQods Ymlahi-Ouazzani, Odile J Bronchain, Elodie Paillard, et al.
Neurogenetics|October 14, 2008
Expression analysis of genes lying in the NF1 microdeletion interval points to four candidate modifiers for neurofibroma formationB Bartelt-Kirbach, M Wuepping, M Dodrimont-Lattke, et al.
Pageof 95

Showing results (631-640 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|September 21, 2010
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variabilityLucio Santoro, Guido J Breedveld, Fiore Manganelli, et al.
Neurogenetics|February 3, 2009
Examination of association of genes in the serotonin system to autismB M Anderson, N C Schnetz-Boutaud, J Bartlett, et al.
Neurogenetics|April 7, 2010
LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Neurogenetics|May 6, 2010
Myotonic dystrophy type I combined with X-linked dominant Charcot-Marie-Tooth neuropathyHyun Sook Kim, Ki Wha Chung, Sung Hee Kang, et al.
Neurogenetics|September 25, 2009
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 geneGabriele Dekomien, Conni Vollrath, Elisabeth Petrasch-Parwez, et al.
Neurogenetics|October 7, 2006
Complex gene-gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genesAlison A Motsinger, David Brassat, Stacy J Caillier, et al.
Neurogenetics|December 18, 2008
Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)Julien Cassereau, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurogenetics|March 12, 2009
The impact of spermine synthase (SMS) mutations on brain morphologyShelli R Kesler, Charles Schwartz, Roger E Stevenson, et al.
Neurogenetics|June 12, 2009
Reduced levels of survival motor neuron protein leads to aberrant motoneuron growth in a Xenopus model of muscular atrophyQods Ymlahi-Ouazzani, Odile J Bronchain, Elodie Paillard, et al.
Neurogenetics|October 14, 2008
Expression analysis of genes lying in the NF1 microdeletion interval points to four candidate modifiers for neurofibroma formationB Bartelt-Kirbach, M Wuepping, M Dodrimont-Lattke, et al.
Pageof 95