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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
November 1, 1994
Use of transvaginal ultrasonography with color Doppler imaging to determine an appropriate treatment regimen for uterine fibroids with a GnRH agonist before surgery: a preliminary study
S Creighton, T H Bourne, F G Lawton, et al.
Biochemistry
|
April 18, 1989
Role of arginine-38 in regulation of the cytochrome c oxidation-reduction equilibrium
R L Cutler, A M Davies, S Creighton, et al.
Molecular Syndromology
|
May 9, 2013
The c.7409G>A (p.Cys2470Tyr) Variant of FBN1: Phenotypic Variability across Three Generations
K J Potter, S Creighton, L Armstrong, et al.
Journal of Biomolecular Structure & Dynamics
|
April 1, 1989
A combined 2D-NMR and molecular dynamics analysis of the structure of the actinomycin D: d(ATGCAT)2 complex
S Creighton, B Rudolph, T Lybrand, et al.
American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses
|
May 6, 1999
Prevalence of leg wound complications after coronary artery bypass grafting: determination of risk factors
M A Goldsborough, M H Miller, J Gibson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 24, 2000
Identification of the human cytochrome P450, P450RAI-2, which is predominantly expressed in the adult cerebellum and is responsible for all-trans-retinoic acid metabolism
J A White, H Ramshaw, M Taimi, et al.
Clinical Genetics
|
March 1, 2005
A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH
C Harvard, P Malenfant, M Koochek, et al.
Clinical Genetics
|
February 21, 2007
Managing genetic discrimination: strategies used by individuals found to have the Huntington disease mutation
Y Bombard, E Penziner, J Decolongon, et al.
Neurology
|
November 10, 2010
Magnetic resonance spectroscopy biomarkers in premanifest and early Huntington disease
A Sturrock, C Laule, J Decolongon, et al.
Clinical Genetics
|
June 6, 2003
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000
S Creighton, E W Almqvist, D MacGregor, et al.
Page
of 6
Search research articles
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Showing results (51-60 of 60) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 60 results.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
November 1, 1994
Use of transvaginal ultrasonography with color Doppler imaging to determine an appropriate treatment regimen for uterine fibroids with a GnRH agonist before surgery: a preliminary study
S Creighton, T H Bourne, F G Lawton, et al.
Biochemistry
|
April 18, 1989
Role of arginine-38 in regulation of the cytochrome c oxidation-reduction equilibrium
R L Cutler, A M Davies, S Creighton, et al.
Molecular Syndromology
|
May 9, 2013
The c.7409G>A (p.Cys2470Tyr) Variant of FBN1: Phenotypic Variability across Three Generations
K J Potter, S Creighton, L Armstrong, et al.
Journal of Biomolecular Structure & Dynamics
|
April 1, 1989
A combined 2D-NMR and molecular dynamics analysis of the structure of the actinomycin D: d(ATGCAT)2 complex
S Creighton, B Rudolph, T Lybrand, et al.
American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses
|
May 6, 1999
Prevalence of leg wound complications after coronary artery bypass grafting: determination of risk factors
M A Goldsborough, M H Miller, J Gibson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 24, 2000
Identification of the human cytochrome P450, P450RAI-2, which is predominantly expressed in the adult cerebellum and is responsible for all-trans-retinoic acid metabolism
J A White, H Ramshaw, M Taimi, et al.
Clinical Genetics
|
March 1, 2005
A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH
C Harvard, P Malenfant, M Koochek, et al.
Clinical Genetics
|
February 21, 2007
Managing genetic discrimination: strategies used by individuals found to have the Huntington disease mutation
Y Bombard, E Penziner, J Decolongon, et al.
Neurology
|
November 10, 2010
Magnetic resonance spectroscopy biomarkers in premanifest and early Huntington disease
A Sturrock, C Laule, J Decolongon, et al.
Clinical Genetics
|
June 6, 2003
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000
S Creighton, E W Almqvist, D MacGregor, et al.
Page
of 6