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T W Prior

Showing results (71-80 of 75) with videos related to

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Human Molecular Genetics|February 3, 2000
The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophyU R Monani, M Sendtner, D D Coovert, et al.
Neurology|February 10, 2010
Mutant small heat shock protein B3 causes motor neuropathy: utility of a candidate gene approachS J Kolb, P J Snyder, E J Poi, et al.
Journal of the Neurological Sciences|October 26, 2001
A placebo-controlled trial of gabapentin in spinal muscular atrophyR G Miller, D H Moore, V Dronsky, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 2, 2001
Comparison of cytogenetic and molecular genetic detection of t(8;21) and inv(16) in a prospective series of adults with de novo acute myeloid leukemia: a Cancer and Leukemia Group B StudyK Mrózek, T W Prior, C Edwards, et al.
Human Genetics|April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.
Pageof 8

Showing results (71-80 of 75) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 75 results.
Human Molecular Genetics|February 3, 2000
The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophyU R Monani, M Sendtner, D D Coovert, et al.
Neurology|February 10, 2010
Mutant small heat shock protein B3 causes motor neuropathy: utility of a candidate gene approachS J Kolb, P J Snyder, E J Poi, et al.
Journal of the Neurological Sciences|October 26, 2001
A placebo-controlled trial of gabapentin in spinal muscular atrophyR G Miller, D H Moore, V Dronsky, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 2, 2001
Comparison of cytogenetic and molecular genetic detection of t(8;21) and inv(16) in a prospective series of adults with de novo acute myeloid leukemia: a Cancer and Leukemia Group B StudyK Mrózek, T W Prior, C Edwards, et al.
Human Genetics|April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.
Pageof 8