Search research articles
Contact Us
Filters
Showing results (11-20 of 104) with videos related to
Page
of 11
Sort By:
Neurology
|
August 10, 2005
Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations
D Zhu, M L Kennerson, G Walizada, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
|
June 1, 1996
Ocular motility in North Carolina autosomal dominant ataxia
K W Small, S C Pollock, J M Vance, et al.
FEBS Letters
|
December 9, 1996
Toxicity of expanded polyglutamine-domain proteins in Escherichia coli
O Onodera, A D Roses, S Tsuji, et al.
American Journal of Medical Genetics
|
February 1, 1985
Segregation and linkage analysis of alpha-N-acetyl-D-glucosaminidase (NAG) levels in a black family
M A Pericak-Vance, J M Vance, R C Elston, et al.
Annals of Human Genetics
|
March 29, 2007
Investigation of the PARK10 gene in Parkinson disease
Y J Li, J Deng, G M Mayhew, et al.
Neurology
|
February 9, 2005
Family-based case-control study of cigarette smoking and Parkinson disease
W K Scott, F Zhang, J M Stajich, et al.
Molecular Vision
|
June 27, 2000
Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes
N P Liu, S Dew-Knight, F Jonasson, et al.
Nucleic Acids Research
|
May 11, 1994
Partitioned pulsed-field gel electrophoresis-PCR (PPF-PCR): a new method for pulsed-field mapping for STS and microsatellites
P H Denton, J B Cullen, D Loeb, et al.
Genomics
|
July 1, 1992
North Carolina macular dystrophy is assigned to chromosome 6
K W Small, J L Weber, A Roses, et al.
Lancet (London, England)
|
December 17, 1994
Dentatorubral-pallidoluysian atrophy and Haw River syndrome
J R Burke, T Ikeuchi, R Koide, et al.
Page
of 11
Search research articles
Search
Showing results (11-20 of 104) with videos related to
Sort By:
Page
of 11
Neurology
|
August 10, 2005
Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations
D Zhu, M L Kennerson, G Walizada, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
|
June 1, 1996
Ocular motility in North Carolina autosomal dominant ataxia
K W Small, S C Pollock, J M Vance, et al.
FEBS Letters
|
December 9, 1996
Toxicity of expanded polyglutamine-domain proteins in Escherichia coli
O Onodera, A D Roses, S Tsuji, et al.
American Journal of Medical Genetics
|
February 1, 1985
Segregation and linkage analysis of alpha-N-acetyl-D-glucosaminidase (NAG) levels in a black family
M A Pericak-Vance, J M Vance, R C Elston, et al.
Annals of Human Genetics
|
March 29, 2007
Investigation of the PARK10 gene in Parkinson disease
Y J Li, J Deng, G M Mayhew, et al.
Neurology
|
February 9, 2005
Family-based case-control study of cigarette smoking and Parkinson disease
W K Scott, F Zhang, J M Stajich, et al.
Molecular Vision
|
June 27, 2000
Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes
N P Liu, S Dew-Knight, F Jonasson, et al.
Nucleic Acids Research
|
May 11, 1994
Partitioned pulsed-field gel electrophoresis-PCR (PPF-PCR): a new method for pulsed-field mapping for STS and microsatellites
P H Denton, J B Cullen, D Loeb, et al.
Genomics
|
July 1, 1992
North Carolina macular dystrophy is assigned to chromosome 6
K W Small, J L Weber, A Roses, et al.
Lancet (London, England)
|
December 17, 1994
Dentatorubral-pallidoluysian atrophy and Haw River syndrome
J R Burke, T Ikeuchi, R Koide, et al.
Page
of 11