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I Gicquel

Showing results (1-10 of 7) with videos related to

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Genomics|January 27, 1998
A 1200-kilobase transcription map encompassing the D6S105 locus at 6p21.3J Mosser, N Andrieux, P Fergelot, et al.
Blood Cells, Molecules & Diseases|September 23, 2000
The HFE gene undergoes alternate splicing processesA Thénié, M Orhant, I Gicquel, et al.
Journal of Endocrinological Investigation|June 16, 2001
Non-hyperfunctioning nodules from multinodular goiters: a minor role in pathogenesis for somatic activating mutations in the TSH-receptor and Gsalpha subunit genesC Derrien, E Sonnet, I Gicquel, et al.
Human Molecular Genetics|January 1, 1993
Localization of seven new genes around the HLA-A locusA el Kahloun, B Chauvel, V Mauvieux, et al.
Human Genetics|October 1, 1986
DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant familyV David, P Paul, M Simon, et al.
Journal of Medical Genetics|October 4, 2005
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeC Bendavid, B R Haddad, A Griffin, et al.
Molecular Syndromology|October 30, 2013
Array-CGH Analysis Suggests Genetic Heterogeneity in RhombencephalosynapsisF Démurger, L Pasquier, C Dubourg, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Genomics|January 27, 1998
A 1200-kilobase transcription map encompassing the D6S105 locus at 6p21.3J Mosser, N Andrieux, P Fergelot, et al.
Blood Cells, Molecules & Diseases|September 23, 2000
The HFE gene undergoes alternate splicing processesA Thénié, M Orhant, I Gicquel, et al.
Journal of Endocrinological Investigation|June 16, 2001
Non-hyperfunctioning nodules from multinodular goiters: a minor role in pathogenesis for somatic activating mutations in the TSH-receptor and Gsalpha subunit genesC Derrien, E Sonnet, I Gicquel, et al.
Human Molecular Genetics|January 1, 1993
Localization of seven new genes around the HLA-A locusA el Kahloun, B Chauvel, V Mauvieux, et al.
Human Genetics|October 1, 1986
DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant familyV David, P Paul, M Simon, et al.
Journal of Medical Genetics|October 4, 2005
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeC Bendavid, B R Haddad, A Griffin, et al.
Molecular Syndromology|October 30, 2013
Array-CGH Analysis Suggests Genetic Heterogeneity in RhombencephalosynapsisF Démurger, L Pasquier, C Dubourg, et al.
Pageof 1