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R J McKinlay Gardner

Showing results (1-10 of 41) with videos related to

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Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 20Elsdon Storey, R J McKinlay Gardner
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 15Elsdon Storey, R J McKinlay Gardner
European Journal of Human Genetics : EJHG|August 30, 2007
Deletions that reveal recessive genesDavid J Coman, R J McKinlay Gardner
Clinical Dysmorphology|September 6, 2007
MURCS and thenar hypoplasiaR J McKinlay Gardner, Mark P Umstad, Lyndon G Hale
Prenatal Diagnosis|April 3, 2012
Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testingGeorge McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, et al.
Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia type 20Elsdon Storey, Melanie A Knight, Susan M Forrest, et al.
Human Mutation|October 3, 2000
Identification of a novel missense mutation L329I in the episodic ataxia type 1 gene KCNA1--a challenging problemM A Knight, E Storey, R J McKinlay Gardner, et al.
Epilepsia|March 21, 2002
Chromosomal abnormalities and epilepsy: a review for clinicians and gene huntersRita Singh, R J McKinlay Gardner, Kathryn M Crossland, et al.
Genetics Research International|September 25, 2013
Diagnostic genetics at a distance: von hippel-lindau disease and a novel mutationClare Brookes, Debra O Prosser, Jennifer M Love, et al.
Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia type 15R J McKinlay Gardner, Melanie A Knight, Kenju Hara, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 20Elsdon Storey, R J McKinlay Gardner
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 15Elsdon Storey, R J McKinlay Gardner
European Journal of Human Genetics : EJHG|August 30, 2007
Deletions that reveal recessive genesDavid J Coman, R J McKinlay Gardner
Clinical Dysmorphology|September 6, 2007
MURCS and thenar hypoplasiaR J McKinlay Gardner, Mark P Umstad, Lyndon G Hale
Prenatal Diagnosis|April 3, 2012
Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testingGeorge McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, et al.
Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia type 20Elsdon Storey, Melanie A Knight, Susan M Forrest, et al.
Human Mutation|October 3, 2000
Identification of a novel missense mutation L329I in the episodic ataxia type 1 gene KCNA1--a challenging problemM A Knight, E Storey, R J McKinlay Gardner, et al.
Epilepsia|March 21, 2002
Chromosomal abnormalities and epilepsy: a review for clinicians and gene huntersRita Singh, R J McKinlay Gardner, Kathryn M Crossland, et al.
Genetics Research International|September 25, 2013
Diagnostic genetics at a distance: von hippel-lindau disease and a novel mutationClare Brookes, Debra O Prosser, Jennifer M Love, et al.
Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia type 15R J McKinlay Gardner, Melanie A Knight, Kenju Hara, et al.
Pageof 5