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S M Huson

Showing results (41-50 of 85) with videos related to

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Journal of Medical Genetics|March 1, 1992
Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1M Upadhyaya, A Fryer, J MacMillan, et al.
Clinical Dysmorphology|July 1, 1996
Three infants of diabetic mothers with malformations of left-right asymmetry--further evidence for the aetiological role of diabetes in this malformation spectrumA Slavotinek, E Hellen, S Gould, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular studyD G Evans, S Mason, S M Huson, et al.
Journal of the Neurological Sciences|May 8, 2000
Diagnostic re-evaluation of a case of 'cerebellar atrophy with Huntington's disease'S M White, S S Gubbay, C G Norbury, et al.
The Journal of Laryngology and Otology|May 1, 1993
Type 2 neurofibromatosis: the need for supraregional care?D G Evans, R Ramsden, S M Huson, et al.
Human Genetics|July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisationR M Winter, K E Davies, M V Bell, et al.
Human Molecular Genetics|December 1, 1992
Analysis of mutations at the neurofibromatosis 1 (NF1) locusM Upadhyaya, M Shen, A Cherryson, et al.
The Quarterly Journal of Medicine|August 1, 1992
A clinical study of type 2 neurofibromatosisD G Evans, S M Huson, D Donnai, et al.
Clinical Genetics|May 2, 2007
Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma?D G R Evans, R T Ramsden, C Gokhale, et al.
Lancet (London, England)|July 1, 1995
Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigenA Vincent, C Newland, L Brueton, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|March 1, 1992
Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1M Upadhyaya, A Fryer, J MacMillan, et al.
Clinical Dysmorphology|July 1, 1996
Three infants of diabetic mothers with malformations of left-right asymmetry--further evidence for the aetiological role of diabetes in this malformation spectrumA Slavotinek, E Hellen, S Gould, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular studyD G Evans, S Mason, S M Huson, et al.
Journal of the Neurological Sciences|May 8, 2000
Diagnostic re-evaluation of a case of 'cerebellar atrophy with Huntington's disease'S M White, S S Gubbay, C G Norbury, et al.
The Journal of Laryngology and Otology|May 1, 1993
Type 2 neurofibromatosis: the need for supraregional care?D G Evans, R Ramsden, S M Huson, et al.
Human Genetics|July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisationR M Winter, K E Davies, M V Bell, et al.
Human Molecular Genetics|December 1, 1992
Analysis of mutations at the neurofibromatosis 1 (NF1) locusM Upadhyaya, M Shen, A Cherryson, et al.
The Quarterly Journal of Medicine|August 1, 1992
A clinical study of type 2 neurofibromatosisD G Evans, S M Huson, D Donnai, et al.
Clinical Genetics|May 2, 2007
Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma?D G R Evans, R T Ramsden, C Gokhale, et al.
Lancet (London, England)|July 1, 1995
Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigenA Vincent, C Newland, L Brueton, et al.
Pageof 9