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N S Thomas

Showing results (41-50 of 133) with videos related to

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Journal of the Neurological Sciences|April 1, 1973
Structural changes in myosin in dystrophic, denervated and regenerating muscle in miceH A John, N S Thomas, P Larson, et al.
Endoscopic Ultrasound|July 1, 2017
Seagulls of endoscopic ultrasoundAmit Pathak, Abid Shoukat, N S Thomas, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A reinvestigation of non-disjunction resulting in 47, XXY males of paternal originN S Thomas, A R Collins, T J Hassold, et al.
Journal of Medical Genetics|December 1, 1986
Molecular deletion analysis in Duchenne muscular dystrophyN S Thomas, P N Ray, R G Worton, et al.
Science (New York, N.Y.)|November 7, 1986
A pseudoautosomal gene in manP J Goodfellow, S M Darling, N S Thomas, et al.
Journal of Molecular Endocrinology|December 16, 2000
p107 is active in the nucleolus in non-dividing human granulosa lutein cellsC Green, R Chatterjee, H H McGarrigle, et al.
Human Genetics|April 1, 1987
X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localizationA Clarke, M Sarfarazi, N S Thomas, et al.
Journal of Medical Genetics|April 1, 1990
Becker muscular dystrophy: correlation of deletion type with clinical severityA M Norman, N S Thomas, H M Kingston, et al.
Blood|July 1, 1997
Characterization of cell cycle status and E2F complexes in mobilized CD34+ cells before and after cytokine stimulationC D Williams, D C Linch, M J Watts, et al.
The British Journal of Ophthalmology|May 1, 1995
Aland island eye disease: clinical and electrophysiological studies of a Welsh familyN R Hawksworth, S Headland, P Good, et al.
Pageof 14

Showing results (41-50 of 133) with videos related to

Sort By:
Pageof 14
Journal of the Neurological Sciences|April 1, 1973
Structural changes in myosin in dystrophic, denervated and regenerating muscle in miceH A John, N S Thomas, P Larson, et al.
Endoscopic Ultrasound|July 1, 2017
Seagulls of endoscopic ultrasoundAmit Pathak, Abid Shoukat, N S Thomas, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A reinvestigation of non-disjunction resulting in 47, XXY males of paternal originN S Thomas, A R Collins, T J Hassold, et al.
Journal of Medical Genetics|December 1, 1986
Molecular deletion analysis in Duchenne muscular dystrophyN S Thomas, P N Ray, R G Worton, et al.
Science (New York, N.Y.)|November 7, 1986
A pseudoautosomal gene in manP J Goodfellow, S M Darling, N S Thomas, et al.
Journal of Molecular Endocrinology|December 16, 2000
p107 is active in the nucleolus in non-dividing human granulosa lutein cellsC Green, R Chatterjee, H H McGarrigle, et al.
Human Genetics|April 1, 1987
X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localizationA Clarke, M Sarfarazi, N S Thomas, et al.
Journal of Medical Genetics|April 1, 1990
Becker muscular dystrophy: correlation of deletion type with clinical severityA M Norman, N S Thomas, H M Kingston, et al.
Blood|July 1, 1997
Characterization of cell cycle status and E2F complexes in mobilized CD34+ cells before and after cytokine stimulationC D Williams, D C Linch, M J Watts, et al.
The British Journal of Ophthalmology|May 1, 1995
Aland island eye disease: clinical and electrophysiological studies of a Welsh familyN R Hawksworth, S Headland, P Good, et al.
Pageof 14