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R Tupler

Showing results (31-40 of 35) with videos related to

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Journal of Medical Genetics|January 1, 1992
Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndromeR Tupler, L Bortotto, E M Bühler, et al.
Anticancer Research|May 1, 1992
Establishment and characterization of two cell lines derived from human glioblastoma multiformeG Bacciocchi, N Gibelli, C Zibera, et al.
Neuroscience Letters|September 14, 1992
A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) geneG Vaula, M Mortilla, R Tupler, et al.
Journal of the Neurological Sciences|October 13, 2010
New molecular findings in congenital myopathies due to selenoprotein N gene mutationsR Cagliani, M E Fruguglietti, A Berardinelli, et al.
Nature|September 13, 1990
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorderP H St George-Hyslop, J L Haines, L A Farrer, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Journal of Medical Genetics|January 1, 1992
Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndromeR Tupler, L Bortotto, E M Bühler, et al.
Anticancer Research|May 1, 1992
Establishment and characterization of two cell lines derived from human glioblastoma multiformeG Bacciocchi, N Gibelli, C Zibera, et al.
Neuroscience Letters|September 14, 1992
A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) geneG Vaula, M Mortilla, R Tupler, et al.
Journal of the Neurological Sciences|October 13, 2010
New molecular findings in congenital myopathies due to selenoprotein N gene mutationsR Cagliani, M E Fruguglietti, A Berardinelli, et al.
Nature|September 13, 1990
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorderP H St George-Hyslop, J L Haines, L A Farrer, et al.
Pageof 4