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L Bruel

Showing results (1-10 of 14) with videos related to

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Applied Optics|September 22, 2010
Comparison of surface and bulk scattering in optical multilayersC Amra, C Grèzes-Besset, L Bruel
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|August 1, 1992
D-glyceraldehyde-3-phosphate dehydrogenase from HeLa cells--1. Purification and properties of the enzymeM Nakano, S Funayama, M B de Oliveira, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|August 1, 1992
D-glyceraldehyde-3-phosphate dehydrogenase from HeLa cells--2. Immunological characterizationE M Gomes, S Funayama, M B de Oliveira, et al.
Applied and Environmental Microbiology|August 28, 2012
Functional analysis of family GH36 α-galactosidases from Ruminococcus gnavus E1: insights into the metabolism of a plant oligosaccharide by a human gut symbiontM Cervera-Tison, L E Tailford, C Fuell, et al.
American Journal of Medical Genetics. Part A|October 27, 2018
TBL1XR1 mutations in Pierpont syndrome are not restricted to the recurrent p.Tyr446Cys mutationC Lemattre, J Thevenon, Y Duffourd, et al.
Clinical Genetics|February 17, 2018
INTU-related oral-facial-digital syndrome type VI: A confirmatory reportA-L Bruel, J Levy, N Elenga, et al.
Clinical Genetics|April 23, 2016
Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesisA-L Bruel, A Masurel-Paulet, J-B Rivière, et al.
Clinical Genetics|February 21, 2018
Truncating variants of the DLG4 gene are responsible for intellectual disability with marfanoid featuresS Moutton, A-L Bruel, M Assoum, et al.
Clinical Genetics|April 11, 2016
Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangiaJ Thevenon, L Duplomb, S Phadke, et al.
Clinical Genetics|February 4, 2017
Further delineation of a rare recessive encephalomyopathy linked to mutations in GFER thanks to data sharing of whole exome sequencing dataS Nambot, D Gavrilov, J Thevenon, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Applied Optics|September 22, 2010
Comparison of surface and bulk scattering in optical multilayersC Amra, C Grèzes-Besset, L Bruel
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|August 1, 1992
D-glyceraldehyde-3-phosphate dehydrogenase from HeLa cells--1. Purification and properties of the enzymeM Nakano, S Funayama, M B de Oliveira, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|August 1, 1992
D-glyceraldehyde-3-phosphate dehydrogenase from HeLa cells--2. Immunological characterizationE M Gomes, S Funayama, M B de Oliveira, et al.
Applied and Environmental Microbiology|August 28, 2012
Functional analysis of family GH36 α-galactosidases from Ruminococcus gnavus E1: insights into the metabolism of a plant oligosaccharide by a human gut symbiontM Cervera-Tison, L E Tailford, C Fuell, et al.
American Journal of Medical Genetics. Part A|October 27, 2018
TBL1XR1 mutations in Pierpont syndrome are not restricted to the recurrent p.Tyr446Cys mutationC Lemattre, J Thevenon, Y Duffourd, et al.
Clinical Genetics|February 17, 2018
INTU-related oral-facial-digital syndrome type VI: A confirmatory reportA-L Bruel, J Levy, N Elenga, et al.
Clinical Genetics|April 23, 2016
Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesisA-L Bruel, A Masurel-Paulet, J-B Rivière, et al.
Clinical Genetics|February 21, 2018
Truncating variants of the DLG4 gene are responsible for intellectual disability with marfanoid featuresS Moutton, A-L Bruel, M Assoum, et al.
Clinical Genetics|April 11, 2016
Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangiaJ Thevenon, L Duplomb, S Phadke, et al.
Clinical Genetics|February 4, 2017
Further delineation of a rare recessive encephalomyopathy linked to mutations in GFER thanks to data sharing of whole exome sequencing dataS Nambot, D Gavrilov, J Thevenon, et al.
Pageof 2