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J B Stephenson

Showing results (71-80 of 110) with videos related to

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Eye (London, England)|January 1, 1988
A familial syndrome with coats' reaction retinal angiomas, hair and nail defects and intracranial calcificationJ L Tolmie, B H Browne, P M McGettrick, et al.
Scottish Medical Journal|August 1, 1988
Vaccine-induced polioencephalomyelitis in ScotlandA A Asindi, E J Bell, M J Browning, et al.
Archives of Disease in Childhood|June 1, 1989
Porencephaly and optic hypoplasia in neonatal isoimmune thrombocytopeniaJ E Davidson, R C McWilliam, T J Evans, et al.
Journal of Medical Genetics|November 1, 1988
Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant traitJ L Tolmie, D E Wilcox, R McWilliam, et al.
American Journal of Medical Genetics|July 1, 1987
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected childJ L Tolmie, M McNay, J B Stephenson, et al.
Cytogenetics and Cell Genetics|January 1, 1987
Tuberous sclerosis: analysis of linkage to red cell and plasma protein markersJ M Connor, J R Yates, L Mann, et al.
Journal of Medical Genetics|January 1, 1989
Genetic aspects of tuberous sclerosis in the west of ScotlandJ R Sampson, S J Scahill, J B Stephenson, et al.
Australian Paediatric Journal|February 1, 1986
Biotin-reversible neurodegenerative disease in infancyL C Low, J B Stephenson, K Bartlett, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Muscle ultrasound in the assessment of suspected neuromuscular disease in childhoodS M Zuberi, N Matta, S Nawaz, et al.
Developmental Medicine and Child Neurology|April 1, 1996
X-linked hydrocephalus masquerading as spina bifida and destructive porencephaly in successive generations in one familyC M Brewer, B J Fredericks, J M Pont, et al.
Pageof 11

Showing results (71-80 of 110) with videos related to

Sort By:
Pageof 11
Eye (London, England)|January 1, 1988
A familial syndrome with coats' reaction retinal angiomas, hair and nail defects and intracranial calcificationJ L Tolmie, B H Browne, P M McGettrick, et al.
Scottish Medical Journal|August 1, 1988
Vaccine-induced polioencephalomyelitis in ScotlandA A Asindi, E J Bell, M J Browning, et al.
Archives of Disease in Childhood|June 1, 1989
Porencephaly and optic hypoplasia in neonatal isoimmune thrombocytopeniaJ E Davidson, R C McWilliam, T J Evans, et al.
Journal of Medical Genetics|November 1, 1988
Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant traitJ L Tolmie, D E Wilcox, R McWilliam, et al.
American Journal of Medical Genetics|July 1, 1987
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected childJ L Tolmie, M McNay, J B Stephenson, et al.
Cytogenetics and Cell Genetics|January 1, 1987
Tuberous sclerosis: analysis of linkage to red cell and plasma protein markersJ M Connor, J R Yates, L Mann, et al.
Journal of Medical Genetics|January 1, 1989
Genetic aspects of tuberous sclerosis in the west of ScotlandJ R Sampson, S J Scahill, J B Stephenson, et al.
Australian Paediatric Journal|February 1, 1986
Biotin-reversible neurodegenerative disease in infancyL C Low, J B Stephenson, K Bartlett, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Muscle ultrasound in the assessment of suspected neuromuscular disease in childhoodS M Zuberi, N Matta, S Nawaz, et al.
Developmental Medicine and Child Neurology|April 1, 1996
X-linked hydrocephalus masquerading as spina bifida and destructive porencephaly in successive generations in one familyC M Brewer, B J Fredericks, J M Pont, et al.
Pageof 11