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S A Robb

Showing results (11-20 of 39) with videos related to

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Human Genetics|November 10, 2001
Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay?T P Kerr, C A Sewry, S A Robb, et al.
European Journal of Pediatrics|October 5, 2001
Hyperkalaemic cardiac arrest in a manifesting carrier of Duchenne muscular dystrophy following general anaesthesiaT P Kerr, A Duward, S V Hodgson, et al.
Archives of Disease in Childhood|January 1, 1989
The 'happy puppet' syndrome of Angelman: review of the clinical featuresS A Robb, K R Pohl, M Baraitser, et al.
Neuromuscular Disorders : NMD|March 7, 2007
Backache in a Duchenne boyM Kinali, R Robinson, A Y Manzur, et al.
Neuropediatrics|February 1, 1993
A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedemaJ O Hourihane, C P Bennett, R Chaudhuri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
The diverse neurological features of Niemann-Pick disease type C: a report of two casesR J Coleman, S A Robb, B D Lake, et al.
Journal of Neuroimmunology|August 1, 1985
Acetylcholine receptor antibodies in the elderly and in Down's syndromeS A Robb, A Vincent, M A McGregor, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2000
Prenatal onset spinal muscular atrophyM J MacLeod, J E Taylor, P W Lunt, et al.
Journal of Medical Genetics|June 1, 1993
Deletion 9p and sex reversalC P Bennett, Z Docherty, S A Robb, et al.
Developmental Medicine and Child Neurology|December 11, 1997
Absence of alpha-sarcoglycan and novel missense mutations in the alpha-sarcoglycan gene in a young British girl with muscular dystrophyR M Quinlivan, S A Robb, C Sewry, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Human Genetics|November 10, 2001
Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay?T P Kerr, C A Sewry, S A Robb, et al.
European Journal of Pediatrics|October 5, 2001
Hyperkalaemic cardiac arrest in a manifesting carrier of Duchenne muscular dystrophy following general anaesthesiaT P Kerr, A Duward, S V Hodgson, et al.
Archives of Disease in Childhood|January 1, 1989
The 'happy puppet' syndrome of Angelman: review of the clinical featuresS A Robb, K R Pohl, M Baraitser, et al.
Neuromuscular Disorders : NMD|March 7, 2007
Backache in a Duchenne boyM Kinali, R Robinson, A Y Manzur, et al.
Neuropediatrics|February 1, 1993
A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedemaJ O Hourihane, C P Bennett, R Chaudhuri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
The diverse neurological features of Niemann-Pick disease type C: a report of two casesR J Coleman, S A Robb, B D Lake, et al.
Journal of Neuroimmunology|August 1, 1985
Acetylcholine receptor antibodies in the elderly and in Down's syndromeS A Robb, A Vincent, M A McGregor, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2000
Prenatal onset spinal muscular atrophyM J MacLeod, J E Taylor, P W Lunt, et al.
Journal of Medical Genetics|June 1, 1993
Deletion 9p and sex reversalC P Bennett, Z Docherty, S A Robb, et al.
Developmental Medicine and Child Neurology|December 11, 1997
Absence of alpha-sarcoglycan and novel missense mutations in the alpha-sarcoglycan gene in a young British girl with muscular dystrophyR M Quinlivan, S A Robb, C Sewry, et al.
Pageof 4