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M MacCollin

Showing results (11-20 of 41) with videos related to

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Annals of Neurology|December 1, 1990
Ataxia and peripheral neuropathy: a benign variant of peroxisome dysgenesisM MacCollin, D C De Vivo, A B Moser, et al.
Journal of the American Academy of Dermatology|January 10, 2001
Familial occurrence of adiposis dolorosaR Campen, H Mankin, D N Louis, et al.
Genes, Chromosomes & Cancer|September 1, 1996
Frequency and distribution of NF2 mutations in schwannomasL B Jacoby, M MacCollin, R Barone, et al.
Neurology|January 1, 1993
Dominantly inherited, early-onset parkinsonism: neuropathology of a new formA J Dwork, C Balmaceda, E A Fazzini, et al.
Clinical Genetics|July 24, 2008
Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosisC Boyd, M J Smith, L Kluwe, et al.
American Journal of Medical Genetics|May 30, 1998
Phenotypic variability associated with 14 splice-site mutations in the NF2 geneL Kluwe, M MacCollin, M Tatagiba, et al.
Radiology|February 13, 2001
Intramedullary and spinal canal tumors in patients with neurofibromatosis 2: MR imaging findings and correlation with genotypeN J Patronas, N Courcoutsakis, C M Bromley, et al.
Human Molecular Genetics|March 1, 1994
The murine NF2 homologue encodes a highly conserved merlin protein with alternative formsV H Haase, J A Trofatter, M MacCollin, et al.
Annals of Neurology|September 1, 1996
A point mutation associated with a severe phenotype of neurofibromatosis 2M MacCollin, N Braverman, D Viskochil, et al.
American Journal of Human Genetics|December 18, 1997
Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosisL B Jacoby, D Jones, K Davis, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Annals of Neurology|December 1, 1990
Ataxia and peripheral neuropathy: a benign variant of peroxisome dysgenesisM MacCollin, D C De Vivo, A B Moser, et al.
Journal of the American Academy of Dermatology|January 10, 2001
Familial occurrence of adiposis dolorosaR Campen, H Mankin, D N Louis, et al.
Genes, Chromosomes & Cancer|September 1, 1996
Frequency and distribution of NF2 mutations in schwannomasL B Jacoby, M MacCollin, R Barone, et al.
Neurology|January 1, 1993
Dominantly inherited, early-onset parkinsonism: neuropathology of a new formA J Dwork, C Balmaceda, E A Fazzini, et al.
Clinical Genetics|July 24, 2008
Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosisC Boyd, M J Smith, L Kluwe, et al.
American Journal of Medical Genetics|May 30, 1998
Phenotypic variability associated with 14 splice-site mutations in the NF2 geneL Kluwe, M MacCollin, M Tatagiba, et al.
Radiology|February 13, 2001
Intramedullary and spinal canal tumors in patients with neurofibromatosis 2: MR imaging findings and correlation with genotypeN J Patronas, N Courcoutsakis, C M Bromley, et al.
Human Molecular Genetics|March 1, 1994
The murine NF2 homologue encodes a highly conserved merlin protein with alternative formsV H Haase, J A Trofatter, M MacCollin, et al.
Annals of Neurology|September 1, 1996
A point mutation associated with a severe phenotype of neurofibromatosis 2M MacCollin, N Braverman, D Viskochil, et al.
American Journal of Human Genetics|December 18, 1997
Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosisL B Jacoby, D Jones, K Davis, et al.
Pageof 5