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Neurogenetics

Showing results (771-780 of 949) with videos related to

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Neurogenetics|March 13, 2017
Alternative outcomes of pathogenic complex somatic structural variations in the genomes of NF1 and NF2 patientsMeng-Chang Hsiao, Arkadiusz Piotrowski, Andrzej Brunon Poplawski, et al.
Neurogenetics|April 10, 2017
Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3Megha N Murthy, Cornelis Blauwendraat, , et al.
Neurogenetics|April 29, 2014
Genetic variants in IL2RA and IL7R affect multiple sclerosis disease risk and progressionAnthony L Traboulsee, Cecily Q Bernales, Jay P Ross, et al.
Neurogenetics|February 24, 2017
ADCY5-related dyskinesia presenting as familial myoclonus-dystoniaAndrew G L Douglas, Gaia Andreoletti, Kevin Talbot, et al.
Neurogenetics|February 13, 2017
Analysis of gene expression in the nervous system identifies key genes and novel candidates for health and diseaseSarah M Carpanini, Thomas M Wishart, Thomas H Gillingwater, et al.
Neurogenetics|March 19, 2004
Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16Luc Djoussé, Beth Knowlton, Michael R Hayden, et al.
Neurogenetics|April 11, 2003
Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralinMireille Lavigne-Rebillard, Benjamin Delprat, Marie-Odile Surget, et al.
Neurogenetics|April 11, 2003
Association of dopamine D4 receptor (DRD4) exon III repeat polymorphism with temperament in 3-year-old infantsAlessandro De Luca, Mario Rizzardi, Anna Buccino, et al.
Neurogenetics|November 5, 2003
Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative studyMargaret A Pericak-Vance, Jackie B Rimmler, Jonathan L Haines, et al.
Neurogenetics|December 3, 2003
Specific mutations in the HEXA gene among Iraqi Jewish Tay-Sachs disease carriers: dating of founder ancestorMazal Karpati, Ephraim Gazit, Boleslaw Goldman, et al.
Pageof 95

Showing results (771-780 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|March 13, 2017
Alternative outcomes of pathogenic complex somatic structural variations in the genomes of NF1 and NF2 patientsMeng-Chang Hsiao, Arkadiusz Piotrowski, Andrzej Brunon Poplawski, et al.
Neurogenetics|April 10, 2017
Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3Megha N Murthy, Cornelis Blauwendraat, , et al.
Neurogenetics|April 29, 2014
Genetic variants in IL2RA and IL7R affect multiple sclerosis disease risk and progressionAnthony L Traboulsee, Cecily Q Bernales, Jay P Ross, et al.
Neurogenetics|February 24, 2017
ADCY5-related dyskinesia presenting as familial myoclonus-dystoniaAndrew G L Douglas, Gaia Andreoletti, Kevin Talbot, et al.
Neurogenetics|February 13, 2017
Analysis of gene expression in the nervous system identifies key genes and novel candidates for health and diseaseSarah M Carpanini, Thomas M Wishart, Thomas H Gillingwater, et al.
Neurogenetics|March 19, 2004
Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16Luc Djoussé, Beth Knowlton, Michael R Hayden, et al.
Neurogenetics|April 11, 2003
Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralinMireille Lavigne-Rebillard, Benjamin Delprat, Marie-Odile Surget, et al.
Neurogenetics|April 11, 2003
Association of dopamine D4 receptor (DRD4) exon III repeat polymorphism with temperament in 3-year-old infantsAlessandro De Luca, Mario Rizzardi, Anna Buccino, et al.
Neurogenetics|November 5, 2003
Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative studyMargaret A Pericak-Vance, Jackie B Rimmler, Jonathan L Haines, et al.
Neurogenetics|December 3, 2003
Specific mutations in the HEXA gene among Iraqi Jewish Tay-Sachs disease carriers: dating of founder ancestorMazal Karpati, Ephraim Gazit, Boleslaw Goldman, et al.
Pageof 95