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J Brockmann

Showing results (71-80 of 73) with videos related to

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Human Molecular Genetics|January 10, 2018
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiencySarah J Brockmann, Axel Freischmidt, Patrick Oeckl, et al.
Brain : a Journal of Neurology|April 19, 2021
A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosisAxel Freischmidt, Anand Goswami, Katharina Limm, et al.
Applied Optics|March 14, 2008
Nonintrusive optical measurements of aircraft engine exhaust emissions and comparison with standard intrusive techniquesK Schäfer, J Heland, D H Lister, et al.
Pageof 8

Showing results (71-80 of 73) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 73 results.
Human Molecular Genetics|January 10, 2018
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiencySarah J Brockmann, Axel Freischmidt, Patrick Oeckl, et al.
Brain : a Journal of Neurology|April 19, 2021
A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosisAxel Freischmidt, Anand Goswami, Katharina Limm, et al.
Applied Optics|March 14, 2008
Nonintrusive optical measurements of aircraft engine exhaust emissions and comparison with standard intrusive techniquesK Schäfer, J Heland, D H Lister, et al.
Pageof 8