Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Déborah Jamet

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|January 7, 2016
Insights into RHCE Molecular Analysis in Samples with Partial D Variants: the Experience of Western FranceYann Fichou, Cédric Le Maréchal, Virginie Scotet, et al.
Transfusion|February 28, 2016
Identification of novel variant A alleles within the ABO geneYann Fichou, Michel Hennion, Isabelle Dupont, et al.
Blood Transfusion = Trasfusione Del Sangue|April 24, 2019
A proposal for a rational transfusion strategy in patients of European and North African descent with weak D type 4.0 and 4.1 phenotypesWilly A Flegel, Thierry Peyrard, Jacques Chiaroni, et al.
Haematologica|September 12, 2006
Beta-thalassemia in the indigenous population of Brittany: identification of three rare mutationsDéborah Jamet, Serge Pissard, Marie-Thérèse Blouch, et al.
Transfusion|April 5, 2013
A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genesYann Fichou, Cédric Le Maréchal, Laurence Bryckaert, et al.
Transfusion|May 23, 2012
Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanismsJian-Min Chen, Yann Fichou, Déborah Jamet, et al.
Transfusion|September 29, 2011
Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare allelesYann Fichou, Cédric Le Maréchal, Laurence Bryckaert, et al.
Transfusion|March 17, 2012
Weak D caused by a founder deletion in the RHD geneYann Fichou, Jian-Min Chen, Cédric Le Maréchal, et al.
Anticancer Research|April 20, 2006
Chromosome 1 abnormalities in multiple myelomaYouna Marzin, Déborah Jamet, Nathalie Douet-Guilbert, et al.
Transfusion|December 12, 2012
Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare allelesYann Fichou, Cédric Le Maréchal, Déborah Jamet, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|January 7, 2016
Insights into RHCE Molecular Analysis in Samples with Partial D Variants: the Experience of Western FranceYann Fichou, Cédric Le Maréchal, Virginie Scotet, et al.
Transfusion|February 28, 2016
Identification of novel variant A alleles within the ABO geneYann Fichou, Michel Hennion, Isabelle Dupont, et al.
Blood Transfusion = Trasfusione Del Sangue|April 24, 2019
A proposal for a rational transfusion strategy in patients of European and North African descent with weak D type 4.0 and 4.1 phenotypesWilly A Flegel, Thierry Peyrard, Jacques Chiaroni, et al.
Haematologica|September 12, 2006
Beta-thalassemia in the indigenous population of Brittany: identification of three rare mutationsDéborah Jamet, Serge Pissard, Marie-Thérèse Blouch, et al.
Transfusion|April 5, 2013
A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genesYann Fichou, Cédric Le Maréchal, Laurence Bryckaert, et al.
Transfusion|May 23, 2012
Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanismsJian-Min Chen, Yann Fichou, Déborah Jamet, et al.
Transfusion|September 29, 2011
Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare allelesYann Fichou, Cédric Le Maréchal, Laurence Bryckaert, et al.
Transfusion|March 17, 2012
Weak D caused by a founder deletion in the RHD geneYann Fichou, Jian-Min Chen, Cédric Le Maréchal, et al.
Anticancer Research|April 20, 2006
Chromosome 1 abnormalities in multiple myelomaYouna Marzin, Déborah Jamet, Nathalie Douet-Guilbert, et al.
Transfusion|December 12, 2012
Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare allelesYann Fichou, Cédric Le Maréchal, Déborah Jamet, et al.
Pageof 2