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Thomas Josse

Showing results (21-30 of 25) with videos related to

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The Journal of Allergy and Clinical Immunology|September 17, 2014
HLA-DRA variants predict penicillin allergy in genome-wide fine-mapping genotypingJean-Louis Guéant, Antonino Romano, Jose-Antonio Cornejo-Garcia, et al.
Ebiomedicine|January 11, 2020
Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic studyAbderrahim Oussalah, Elise Jeannesson-Thivisol, Céline Chéry, et al.
Nature Communications|February 4, 2018
Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.
Nature Communications|January 6, 2018
APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.
Oncotarget|October 4, 2017
<i>BRIP1</i> coding variants are associated with a high risk of hepatocellular carcinoma occurrence in patients with HCV- or HBV-related liver diseaseAbderrahim Oussalah, Patrice Hodonou Avogbe, Erwan Guyot, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
The Journal of Allergy and Clinical Immunology|September 17, 2014
HLA-DRA variants predict penicillin allergy in genome-wide fine-mapping genotypingJean-Louis Guéant, Antonino Romano, Jose-Antonio Cornejo-Garcia, et al.
Ebiomedicine|January 11, 2020
Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic studyAbderrahim Oussalah, Elise Jeannesson-Thivisol, Céline Chéry, et al.
Nature Communications|February 4, 2018
Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.
Nature Communications|January 6, 2018
APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.
Oncotarget|October 4, 2017
<i>BRIP1</i> coding variants are associated with a high risk of hepatocellular carcinoma occurrence in patients with HCV- or HBV-related liver diseaseAbderrahim Oussalah, Patrice Hodonou Avogbe, Erwan Guyot, et al.
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