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C Férec

Showing results (1-10 of 110) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 17, 2020
Genetics of cystic fibrosis: BasicsC Férec, V Scotet
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|June 25, 2017
NGS and blood group systems: State of the art and perspectivesY Fichou, C Férec
Molecular Human Reproduction|September 1, 1996
Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferensM De Braekeleer, C Férec
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|July 4, 2017
From genetic variability to phenotypic expression of blood group systemsL Raud, C Férec, Y Fichou
Blood|April 9, 1999
HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosisC Mura, O Raguenes, C Férec
Journal of Virological Methods|February 24, 1999
Simultaneous screening for HBV DNA and HCV RNA genomes in blood donations using a novel TaqMan PCR assayB Mercier, L Burlot, C Férec
Clinical Chemistry|August 22, 2001
Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLCG Le Gac, C Mura, C Férec
Human Genetics|November 10, 2001
Molecular pathology and evolutionary and physiological implications of pancreatitis-associated cationic trypsinogen mutationsJ M Chen, T Montier, C Férec
Transfusion Medicine (Oxford, England)|January 25, 2014
The RHD*weak D type 4.0 allele is predominantly but not exclusively cis-associated with the altered RHCE*ce(c.48C, c.105T, c.733G, c.744C, c.1025T) allele in the French populationY Fichou, C L Maréchal, C Férec
Clinical Genetics|June 24, 2010
Revealing the human mutomeJ M Chen, C Férec, D N Cooper
Pageof 11

Showing results (1-10 of 110) with videos related to

Sort By:
Pageof 11
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 17, 2020
Genetics of cystic fibrosis: BasicsC Férec, V Scotet
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|June 25, 2017
NGS and blood group systems: State of the art and perspectivesY Fichou, C Férec
Molecular Human Reproduction|September 1, 1996
Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferensM De Braekeleer, C Férec
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|July 4, 2017
From genetic variability to phenotypic expression of blood group systemsL Raud, C Férec, Y Fichou
Blood|April 9, 1999
HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosisC Mura, O Raguenes, C Férec
Journal of Virological Methods|February 24, 1999
Simultaneous screening for HBV DNA and HCV RNA genomes in blood donations using a novel TaqMan PCR assayB Mercier, L Burlot, C Férec
Clinical Chemistry|August 22, 2001
Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLCG Le Gac, C Mura, C Férec
Human Genetics|November 10, 2001
Molecular pathology and evolutionary and physiological implications of pancreatitis-associated cationic trypsinogen mutationsJ M Chen, T Montier, C Férec
Transfusion Medicine (Oxford, England)|January 25, 2014
The RHD*weak D type 4.0 allele is predominantly but not exclusively cis-associated with the altered RHCE*ce(c.48C, c.105T, c.733G, c.744C, c.1025T) allele in the French populationY Fichou, C L Maréchal, C Férec
Clinical Genetics|June 24, 2010
Revealing the human mutomeJ M Chen, C Férec, D N Cooper
Pageof 11