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American Journal of Human Genetics
|
June 1, 1992
Recombination of 4p16 DNA markers in an unusual family with Huntington disease
C Pritchard, N Zhu, J Zuo, et al.
Genomics
|
July 20, 1995
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A
K B Othmane, D Loeb, R Hayworth-Hodgte, et al.
Human Molecular Genetics
|
October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
K Ben Othmane, F Hentati, F Lennon, et al.
Genomics
|
March 1, 1990
Confirmation of linkage in von Hippel-Lindau disease
J M Vance, K W Small, M A Jones, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Linkage studies in familial Alzheimer's disease
A D Roses, M A Pericak-Vance, L Yamaoka, et al.
Annals of the New York Academy of Sciences
|
January 1, 1991
Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!
R S Kandt, M A Pericak-Vance, W Y Hung, et al.
Annals of Neurology
|
May 1, 1997
Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhage
M J Alberts, J P Davis, C Graffagnino, et al.
The Pharmacogenomics Journal
|
August 11, 2004
Identification of a pharmacogenetic effect by linkage disequilibrium mapping
C-F Xu, K F Lewis, A J Yeo, et al.
Journal of Medical Genetics
|
September 1, 1987
Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8
S R Diehl, M Boehnke, F S Collins, et al.
Arzneimittel-Forschung
|
March 1, 1995
Influence of the susceptibility genes apolipoprotein E-epsilon 4 and apolipoprotein E-epsilon 2 on the rate of disease expressivity of late-onset Alzheimer's disease
A D Roses, A M Saunders, E H Corder, et al.
Page
of 35
Search research articles
Search
Showing results (251-260 of 347) with videos related to
Sort By:
Page
of 35
American Journal of Human Genetics
|
June 1, 1992
Recombination of 4p16 DNA markers in an unusual family with Huntington disease
C Pritchard, N Zhu, J Zuo, et al.
Genomics
|
July 20, 1995
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A
K B Othmane, D Loeb, R Hayworth-Hodgte, et al.
Human Molecular Genetics
|
October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
K Ben Othmane, F Hentati, F Lennon, et al.
Genomics
|
March 1, 1990
Confirmation of linkage in von Hippel-Lindau disease
J M Vance, K W Small, M A Jones, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Linkage studies in familial Alzheimer's disease
A D Roses, M A Pericak-Vance, L Yamaoka, et al.
Annals of the New York Academy of Sciences
|
January 1, 1991
Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!
R S Kandt, M A Pericak-Vance, W Y Hung, et al.
Annals of Neurology
|
May 1, 1997
Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhage
M J Alberts, J P Davis, C Graffagnino, et al.
The Pharmacogenomics Journal
|
August 11, 2004
Identification of a pharmacogenetic effect by linkage disequilibrium mapping
C-F Xu, K F Lewis, A J Yeo, et al.
Journal of Medical Genetics
|
September 1, 1987
Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8
S R Diehl, M Boehnke, F S Collins, et al.
Arzneimittel-Forschung
|
March 1, 1995
Influence of the susceptibility genes apolipoprotein E-epsilon 4 and apolipoprotein E-epsilon 2 on the rate of disease expressivity of late-onset Alzheimer's disease
A D Roses, A M Saunders, E H Corder, et al.
Page
of 35