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Human Molecular Genetics
|
September 1, 1993
Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1
G Cancel, C Khati, G Stevanin, et al.
Genomics
|
May 15, 1994
Report of the Second International Workshop on Human Chromosome 6
A Volz, J M Boyle, H M Cann, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 9, 1982
3-hydroxy-3-methylglutaric aciduria: a new assay of 3-hydroxy-3-methylglutaryl-coa lyase using high performance liquid chromatography
K M Gibson, L Sweetman, W L Nyhan, et al.
Pediatric Research
|
January 1, 1974
Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency
A S Goldstein, N J Hoogenraad, J D Johnson, et al.
Genomics
|
March 1, 1991
A centromere-based genetic map of the short arm of human chromosome 6
H Blanché, H Y Zoghbi, E W Jabs, et al.
American Journal of Human Genetics
|
January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2
G Stevanin, G Cancel, A Dürr, et al.
Journal of Neurogenetics
|
April 1, 1984
3-Hydroxy-3-methylglutaric aciduria
C L Greene, H M Cann, B H Robinson, et al.
Thrombosis Et Diathesis Haemorrhagica
|
September 15, 1973
A genetic nomenclature for human blood coagulation
J B Graham, D A Barrett, B Blombäck, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping
|
January 1, 1997
Third single chromosome 6 workshop: meeting report
S Beck, H M Cann, R D Campbell, et al.
American Journal of Human Genetics
|
October 1, 1995
Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus
G Cancel, N Abbas, G Stevanin, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
Human Molecular Genetics
|
September 1, 1993
Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1
G Cancel, C Khati, G Stevanin, et al.
Genomics
|
May 15, 1994
Report of the Second International Workshop on Human Chromosome 6
A Volz, J M Boyle, H M Cann, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 9, 1982
3-hydroxy-3-methylglutaric aciduria: a new assay of 3-hydroxy-3-methylglutaryl-coa lyase using high performance liquid chromatography
K M Gibson, L Sweetman, W L Nyhan, et al.
Pediatric Research
|
January 1, 1974
Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency
A S Goldstein, N J Hoogenraad, J D Johnson, et al.
Genomics
|
March 1, 1991
A centromere-based genetic map of the short arm of human chromosome 6
H Blanché, H Y Zoghbi, E W Jabs, et al.
American Journal of Human Genetics
|
January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2
G Stevanin, G Cancel, A Dürr, et al.
Journal of Neurogenetics
|
April 1, 1984
3-Hydroxy-3-methylglutaric aciduria
C L Greene, H M Cann, B H Robinson, et al.
Thrombosis Et Diathesis Haemorrhagica
|
September 15, 1973
A genetic nomenclature for human blood coagulation
J B Graham, D A Barrett, B Blombäck, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping
|
January 1, 1997
Third single chromosome 6 workshop: meeting report
S Beck, H M Cann, R D Campbell, et al.
American Journal of Human Genetics
|
October 1, 1995
Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus
G Cancel, N Abbas, G Stevanin, et al.
Page
of 5