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M T Rogers

Showing results (1-10 of 15) with videos related to

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Leprosy Review|March 1, 1984
Leprosy and the eyeM T Rogers
Journal of the American Chemical Society|March 19, 2010
The magnetic anisotropy of coronene, naphthazarin, and other crystalsM T ROGERS
Journal of the American Chemical Society|October 29, 2010
Cyclopropane derivatives; the electric moments of some alicyclic compoundsM T ROGERS, J D ROBERTS
Clinical Genetics|September 13, 2006
Variability and inequity in testing of somatic tissue for hereditary cancer: a survey of UK clinical practiceC L Gaff, M T Rogers, I M Frayling
Clinical Genetics|May 11, 2007
Genetic counselling and consent for tumour testing in HNPCCC L Gaff, M T Rogers, I M Frayling
Brain : a Journal of Neurology|September 1, 1999
Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia. A clinical and molecular genetic study of 28 United Kingdom familiesE Reid, C Grayson, M T Rogers, et al.
Journal of Medical Genetics|October 21, 1999
Subclinical cognitive impairment in autosomal dominant "pure" hereditary spastic paraplegiaE Reid, C Grayson, D C Rubinsztein, et al.
American Journal of Human Genetics|March 21, 2000
A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13E Reid, A M Dearlove, O Osborn, et al.
Neuromuscular Disorders : NMD|March 27, 1999
Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reportsK M Bushby, C Pollitt, M A Johnson, et al.
Journal of Medical Genetics|June 1, 1997
Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHDM Upadhyaya, J Maynard, M T Rogers, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Leprosy Review|March 1, 1984
Leprosy and the eyeM T Rogers
Journal of the American Chemical Society|March 19, 2010
The magnetic anisotropy of coronene, naphthazarin, and other crystalsM T ROGERS
Journal of the American Chemical Society|October 29, 2010
Cyclopropane derivatives; the electric moments of some alicyclic compoundsM T ROGERS, J D ROBERTS
Clinical Genetics|September 13, 2006
Variability and inequity in testing of somatic tissue for hereditary cancer: a survey of UK clinical practiceC L Gaff, M T Rogers, I M Frayling
Clinical Genetics|May 11, 2007
Genetic counselling and consent for tumour testing in HNPCCC L Gaff, M T Rogers, I M Frayling
Brain : a Journal of Neurology|September 1, 1999
Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia. A clinical and molecular genetic study of 28 United Kingdom familiesE Reid, C Grayson, M T Rogers, et al.
Journal of Medical Genetics|October 21, 1999
Subclinical cognitive impairment in autosomal dominant "pure" hereditary spastic paraplegiaE Reid, C Grayson, D C Rubinsztein, et al.
American Journal of Human Genetics|March 21, 2000
A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13E Reid, A M Dearlove, O Osborn, et al.
Neuromuscular Disorders : NMD|March 27, 1999
Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reportsK M Bushby, C Pollitt, M A Johnson, et al.
Journal of Medical Genetics|June 1, 1997
Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHDM Upadhyaya, J Maynard, M T Rogers, et al.
Pageof 2