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American Journal of Human Genetics
|
September 1, 1996
Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities
D M Parry, M M MacCollin, M I Kaiser-Kupfer, et al.
Somatic Cell and Molecular Genetics
|
January 27, 1999
Genetic variation in the 3' untranslated region of the neurofibromatosis 1 gene: application to unequal allelic expression
G S Cowley, A E Murthy, D M Parry, et al.
Cancer Research
|
January 1, 1994
Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas
M P Rubio, K M Correa, V Ramesh, et al.
American Journal of Human Genetics
|
August 1, 1994
Mutational analysis of patients with neurofibromatosis 2
M MacCollin, V Ramesh, L B Jacoby, et al.
American Journal of Human Genetics
|
July 27, 2001
Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomas suggests different genetic mechanisms for pathogenesis of TSC lesions
Y Niida, A O Stemmer-Rachamimov, M Logrip, et al.
Cell
|
March 12, 1993
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
J A Trofatter, M M MacCollin, J L Rutter, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism
C J Danpure, P Fryer, S Griffiths, et al.
Neurology
|
September 11, 2002
Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1)
D H Gutmann, S A Rasmussen, P Wolkenstein, et al.
Acta Neuropathologica
|
January 29, 2000
Schwann cell-onion bulb tumor of the trigeminal nerve: hyperplasia, dysplasia or neoplasia?
S F LaPoint, J M Powers, J M Woodruff, et al.
Neurology
|
June 16, 2005
Diagnostic criteria for schwannomatosis
M MacCollin, E A Chiocca, D G Evans, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
American Journal of Human Genetics
|
September 1, 1996
Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities
D M Parry, M M MacCollin, M I Kaiser-Kupfer, et al.
Somatic Cell and Molecular Genetics
|
January 27, 1999
Genetic variation in the 3' untranslated region of the neurofibromatosis 1 gene: application to unequal allelic expression
G S Cowley, A E Murthy, D M Parry, et al.
Cancer Research
|
January 1, 1994
Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas
M P Rubio, K M Correa, V Ramesh, et al.
American Journal of Human Genetics
|
August 1, 1994
Mutational analysis of patients with neurofibromatosis 2
M MacCollin, V Ramesh, L B Jacoby, et al.
American Journal of Human Genetics
|
July 27, 2001
Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomas suggests different genetic mechanisms for pathogenesis of TSC lesions
Y Niida, A O Stemmer-Rachamimov, M Logrip, et al.
Cell
|
March 12, 1993
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
J A Trofatter, M M MacCollin, J L Rutter, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism
C J Danpure, P Fryer, S Griffiths, et al.
Neurology
|
September 11, 2002
Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1)
D H Gutmann, S A Rasmussen, P Wolkenstein, et al.
Acta Neuropathologica
|
January 29, 2000
Schwann cell-onion bulb tumor of the trigeminal nerve: hyperplasia, dysplasia or neoplasia?
S F LaPoint, J M Powers, J M Woodruff, et al.
Neurology
|
June 16, 2005
Diagnostic criteria for schwannomatosis
M MacCollin, E A Chiocca, D G Evans, et al.
Page
of 5