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Genomics
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January 15, 1994
Precise mapping of the brain alpha 2-adrenergic receptor gene within chromosome 4p16
O Riess, U Thies, I Siedlaczck, et al.
Human Genetics
|
August 1, 1994
Geographical distribution of haplotypes in Swedish families with Huntington's disease
E Almqvist, S Andrew, J Theilmann, et al.
IEEE Transactions on Medical Imaging
|
November 10, 2001
Chemical-shift imaging utilizing the positional shifts along the readout gradient direction
M I Altbach, T P Trouard, R Van de Walle, et al.
Clinical Genetics
|
June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease
S Andrew, J Theilmann, E Almqvist, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
December 14, 2023
Upper airway imaging and function in obstructive sleep apnea in people with and without HIV
Chantal Darquenne, Rebecca J Theilmann, Ines Rivoalen, et al.
Brain and Cognition
|
March 19, 2008
Microstructural integrity of the corpus callosum linked with neuropsychological performance in adolescents
Susanna L Fryer, Lawrence R Frank, Andrea D Spadoni, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
November 28, 2014
Inhaled nitric oxide alters the distribution of blood flow in the healthy human lung, suggesting active hypoxic pulmonary vasoconstriction in normoxia
Amran K Asadi, Rui Carlos Sá, Nick H Kim, et al.
American Journal of Human Genetics
|
May 1, 1994
Huntington disease without CAG expansion: phenocopies or errors in assignment?
S E Andrew, Y P Goldberg, B Kremer, et al.
Human Molecular Genetics
|
December 1, 1994
DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence
F Squitieri, S E Andrew, Y P Goldberg, et al.
Human Molecular Genetics
|
October 1, 1993
Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent
H Telenius, H P Kremer, J Theilmann, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 96) with videos related to
Sort By:
Page
of 10
Genomics
|
January 15, 1994
Precise mapping of the brain alpha 2-adrenergic receptor gene within chromosome 4p16
O Riess, U Thies, I Siedlaczck, et al.
Human Genetics
|
August 1, 1994
Geographical distribution of haplotypes in Swedish families with Huntington's disease
E Almqvist, S Andrew, J Theilmann, et al.
IEEE Transactions on Medical Imaging
|
November 10, 2001
Chemical-shift imaging utilizing the positional shifts along the readout gradient direction
M I Altbach, T P Trouard, R Van de Walle, et al.
Clinical Genetics
|
June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease
S Andrew, J Theilmann, E Almqvist, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
December 14, 2023
Upper airway imaging and function in obstructive sleep apnea in people with and without HIV
Chantal Darquenne, Rebecca J Theilmann, Ines Rivoalen, et al.
Brain and Cognition
|
March 19, 2008
Microstructural integrity of the corpus callosum linked with neuropsychological performance in adolescents
Susanna L Fryer, Lawrence R Frank, Andrea D Spadoni, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
November 28, 2014
Inhaled nitric oxide alters the distribution of blood flow in the healthy human lung, suggesting active hypoxic pulmonary vasoconstriction in normoxia
Amran K Asadi, Rui Carlos Sá, Nick H Kim, et al.
American Journal of Human Genetics
|
May 1, 1994
Huntington disease without CAG expansion: phenocopies or errors in assignment?
S E Andrew, Y P Goldberg, B Kremer, et al.
Human Molecular Genetics
|
December 1, 1994
DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence
F Squitieri, S E Andrew, Y P Goldberg, et al.
Human Molecular Genetics
|
October 1, 1993
Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent
H Telenius, H P Kremer, J Theilmann, et al.
Page
of 10