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Human Molecular Genetics|March 1, 1994
Exon scanning for mutation of the NF2 gene in schwannomasL B Jacoby, M MacCollin, D N Louis, et al.
Journal of Neuropathology and Experimental Neurology|November 18, 2009
Genomic profiling of atypical meningiomas associates gain of 1q with poor clinical outcomeDarlene Gabeau-Lacet, David Engler, Sumeet Gupta, et al.
International Journal of Radiation Oncology, Biology, Physics|October 6, 2000
Allelic loss of chromosome 1p and radiotherapy plus chemotherapy in patients with oligodendrogliomasG S Bauman, Y Ino, K Ueki, 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 lesionsY Niida, A O Stemmer-Rachamimov, M Logrip, et al.
Cancer Genetics and Cytogenetics|June 1, 1996
The BAX gene maps to the glioma candidate region at 19q13.3, but is not altered in human gliomasD Chou, T Miyashita, H W Mohrenweiser, et al.
Human Gene Therapy|June 14, 2003
Potentiated gene delivery to tumors using herpes simplex virus/Epstein-Barr virus/RV tribrid amplicon vectorsJürgen A Hampl, Sara M Camp, Wojciech K Mydlarz, et al.
Acta Neuropathologica|April 20, 2001
Developmental expression of the tuberous sclerosis proteins tuberin and hamartinV Murthy, A O Stemmer-Rachamimov, L A Haddad, et al.
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