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D Viskochil

Showing results (11-20 of 38) with videos related to

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American Journal of Medical Genetics|September 24, 1999
X-linked lissencephaly with absent corpus callosum and ambiguous genitaliaW B Dobyns, E Berry-Kravis, N J Havernick, et al.
American Journal of Medical Genetics|December 18, 1996
Familial ring (19) chromosome mosaicism: case report and reviewW L Flejter, D Finlinson, S Root, et al.
Annals of the New York Academy of Sciences|January 1, 1991
The NF1 translocation breakpoint regionP O'Connell, R M Cawthon, D Viskochil, 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.
Molecular and Cellular Biology|February 1, 1991
The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 geneD Viskochil, R Cawthon, P O'Connell, et al.
Neurology|June 4, 2002
Plexiform neurofibromas in NF1: toward biologic-based therapyR J Packer, D H Gutmann, A Rubenstein, et al.
Prenatal Diagnosis|October 1, 1993
Preaxial ray reduction defects as part of valproic acid embryofetopathyR Sharony, A Garber, D Viskochil, et al.
JAMA|July 2, 1997
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2D H Gutmann, A Aylsworth, J C Carey, et al.
Cytogenetics and Cell Genetics|January 1, 1996
The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridizationK A Leppig, D Viskochil, S Neil, et al.
The Journal of Clinical Investigation|May 3, 2000
Epidermal growth factor receptor expression in neurofibromatosis type 1-related tumors and NF1 animal modelsJ E DeClue, S Heffelfinger, G Benvenuto, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|September 24, 1999
X-linked lissencephaly with absent corpus callosum and ambiguous genitaliaW B Dobyns, E Berry-Kravis, N J Havernick, et al.
American Journal of Medical Genetics|December 18, 1996
Familial ring (19) chromosome mosaicism: case report and reviewW L Flejter, D Finlinson, S Root, et al.
Annals of the New York Academy of Sciences|January 1, 1991
The NF1 translocation breakpoint regionP O'Connell, R M Cawthon, D Viskochil, 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.
Molecular and Cellular Biology|February 1, 1991
The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 geneD Viskochil, R Cawthon, P O'Connell, et al.
Neurology|June 4, 2002
Plexiform neurofibromas in NF1: toward biologic-based therapyR J Packer, D H Gutmann, A Rubenstein, et al.
Prenatal Diagnosis|October 1, 1993
Preaxial ray reduction defects as part of valproic acid embryofetopathyR Sharony, A Garber, D Viskochil, et al.
JAMA|July 2, 1997
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2D H Gutmann, A Aylsworth, J C Carey, et al.
Cytogenetics and Cell Genetics|January 1, 1996
The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridizationK A Leppig, D Viskochil, S Neil, et al.
The Journal of Clinical Investigation|May 3, 2000
Epidermal growth factor receptor expression in neurofibromatosis type 1-related tumors and NF1 animal modelsJ E DeClue, S Heffelfinger, G Benvenuto, et al.
Pageof 4