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T Strachan

Showing results (91-100 of 138) with videos related to

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Human Molecular Genetics|July 1, 1994
PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouseM Tassabehji, V E Newton, K Leverton, et al.
Neurology|July 1, 1995
Presymptomatic DNA and MRI diagnosis of neurofibromatosis 2 with mild clinical course in an extended pedigreeM Sainio, T Strachan, G Blomstedt, et al.
Journal of Medical Genetics|April 1, 1989
Molecular genetics in the National Health Service in BritainR Harris, R Elles, D Craufurd, et al.
Genomics|April 1, 1996
Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2pR Bashir, S Keers, T Strachan, et al.
Medical and Pediatric Oncology|July 24, 2001
Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastomaM Lastowska, N Van Roy, N Bown, et al.
Immunogenetics|January 1, 1986
Transfection of murine LMTK- cells with purified HLA class I genes. VII. Association of allele- and locus-specific serological reactivities with respectively the first and second domains of the HLA-B7 moleculeR Sodoyer, B Kahn-Perles, T Strachan, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The molecular biology of LGMD2B--towards the identification of the LGMD gene on chromosome 2p13K Bushby, R Bashir, S Keers, et al.
Nature Genetics|September 1, 1995
A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36S A Lynch, P M Bond, A J Copp, et al.
The Journal of Laryngology and Otology|July 1, 1996
A clinical, genetic and audiological study of patients and families with unilateral vestibular schwannomas. I. Clinical features of neurofibromatosis in patients with unilateral vestibular schwannomasW J Neary, V E Newton, S N Laoide-Kemp, et al.
Journal of Medical Genetics|December 1, 1992
A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severityD G Evans, S M Huson, D Donnai, et al.
Pageof 14

Showing results (91-100 of 138) with videos related to

Sort By:
Pageof 14
Human Molecular Genetics|July 1, 1994
PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouseM Tassabehji, V E Newton, K Leverton, et al.
Neurology|July 1, 1995
Presymptomatic DNA and MRI diagnosis of neurofibromatosis 2 with mild clinical course in an extended pedigreeM Sainio, T Strachan, G Blomstedt, et al.
Journal of Medical Genetics|April 1, 1989
Molecular genetics in the National Health Service in BritainR Harris, R Elles, D Craufurd, et al.
Genomics|April 1, 1996
Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2pR Bashir, S Keers, T Strachan, et al.
Medical and Pediatric Oncology|July 24, 2001
Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastomaM Lastowska, N Van Roy, N Bown, et al.
Immunogenetics|January 1, 1986
Transfection of murine LMTK- cells with purified HLA class I genes. VII. Association of allele- and locus-specific serological reactivities with respectively the first and second domains of the HLA-B7 moleculeR Sodoyer, B Kahn-Perles, T Strachan, et al.
Neuromuscular Disorders : NMD|December 1, 1996
The molecular biology of LGMD2B--towards the identification of the LGMD gene on chromosome 2p13K Bushby, R Bashir, S Keers, et al.
Nature Genetics|September 1, 1995
A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36S A Lynch, P M Bond, A J Copp, et al.
The Journal of Laryngology and Otology|July 1, 1996
A clinical, genetic and audiological study of patients and families with unilateral vestibular schwannomas. I. Clinical features of neurofibromatosis in patients with unilateral vestibular schwannomasW J Neary, V E Newton, S N Laoide-Kemp, et al.
Journal of Medical Genetics|December 1, 1992
A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severityD G Evans, S M Huson, D Donnai, et al.
Pageof 14