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Journal of Neurosurgery. Case Lessons
|
October 23, 2022
Xenotransplantation of porcine progenitor cells in an epileptic California sea lion (Zalophus californianus): illustrative case
Claire A Simeone, John P Andrews, Shawn P Johnson, et al.
Brain : a Journal of Neurology
|
March 8, 2008
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study
Ines Dierick, Jonathan Baets, Joy Irobi, et al.
Brain : a Journal of Neurology
|
August 16, 2011
Genetic spectrum of hereditary neuropathies with onset in the first year of life
Jonathan Baets, Tine Deconinck, Els De Vriendt, et al.
Forensic Science International. Synergy
|
July 18, 2025
National Technology Validation and Implementation Collaborative (NTVIC): Updated guidelines for establishing Forensic Investigative Genetic Genealogy (FIGG) programs
Ray A Wickenheiser, Jennifer Naugle, Brian Hoey, et al.
American Journal of Human Genetics
|
December 3, 2014
Truncating and missense mutations in IGHMBP2 cause Charcot-Marie Tooth disease type 2
Ellen Cottenie, Andrzej Kochanski, Albena Jordanova, et al.
Brain : a Journal of Neurology
|
May 23, 2006
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, et al.
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of 12
Search research articles
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Showing results (111-120 of 116) with videos related to
Sort By:
Page
of 12
You have reached the last page of results.
This site can display upto 116 results.
Journal of Neurosurgery. Case Lessons
|
October 23, 2022
Xenotransplantation of porcine progenitor cells in an epileptic California sea lion (Zalophus californianus): illustrative case
Claire A Simeone, John P Andrews, Shawn P Johnson, et al.
Brain : a Journal of Neurology
|
March 8, 2008
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study
Ines Dierick, Jonathan Baets, Joy Irobi, et al.
Brain : a Journal of Neurology
|
August 16, 2011
Genetic spectrum of hereditary neuropathies with onset in the first year of life
Jonathan Baets, Tine Deconinck, Els De Vriendt, et al.
Forensic Science International. Synergy
|
July 18, 2025
National Technology Validation and Implementation Collaborative (NTVIC): Updated guidelines for establishing Forensic Investigative Genetic Genealogy (FIGG) programs
Ray A Wickenheiser, Jennifer Naugle, Brian Hoey, et al.
American Journal of Human Genetics
|
December 3, 2014
Truncating and missense mutations in IGHMBP2 cause Charcot-Marie Tooth disease type 2
Ellen Cottenie, Andrzej Kochanski, Albena Jordanova, et al.
Brain : a Journal of Neurology
|
May 23, 2006
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, et al.
Page
of 12