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P Brouillard

Showing results (11-20 of 17) with videos related to

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European Journal of Medical Genetics|April 22, 2015
Antenatal presentation of hereditary lymphedema type IE Boudon, Y Levy, T Abossolo, et al.
American Journal of Human Genetics|June 12, 1999
A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22L M Boon, P Brouillard, A Irrthum, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Linkage disequilibrium narrows locus for venous malformation with glomus cells (VMGLOM) to a single 1.48 Mbp YACA Irrthum, P Brouillard, O Enjolras, et al.
Journal of Molecular Biology|February 17, 2007
Crystal structure of the streptococcal superantigen SpeI and functional role of a novel loop domain in T cell activation by group V superantigensJean-Nicholas P Brouillard, Sebastian Günther, Ashok K Varma, et al.
Molecular Syndromology|October 30, 2013
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedemaA Mendola, M J Schlögel, A Ghalamkarpour, et al.
Journal of Medical Genetics|February 4, 2005
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effectP Brouillard, M Ghassibé, A Penington, et al.
Molecular Syndromology|June 27, 2013
Genotypes and phenotypes of 162 families with a glomulin mutationP Brouillard, L M Boon, N Revencu, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
European Journal of Medical Genetics|April 22, 2015
Antenatal presentation of hereditary lymphedema type IE Boudon, Y Levy, T Abossolo, et al.
American Journal of Human Genetics|June 12, 1999
A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22L M Boon, P Brouillard, A Irrthum, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Linkage disequilibrium narrows locus for venous malformation with glomus cells (VMGLOM) to a single 1.48 Mbp YACA Irrthum, P Brouillard, O Enjolras, et al.
Journal of Molecular Biology|February 17, 2007
Crystal structure of the streptococcal superantigen SpeI and functional role of a novel loop domain in T cell activation by group V superantigensJean-Nicholas P Brouillard, Sebastian Günther, Ashok K Varma, et al.
Molecular Syndromology|October 30, 2013
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedemaA Mendola, M J Schlögel, A Ghalamkarpour, et al.
Journal of Medical Genetics|February 4, 2005
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effectP Brouillard, M Ghassibé, A Penington, et al.
Molecular Syndromology|June 27, 2013
Genotypes and phenotypes of 162 families with a glomulin mutationP Brouillard, L M Boon, N Revencu, et al.
Pageof 2