Search research articles
Contact Us
Filters
Showing results (1-10 of 110) with videos related to
Page
of 11
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 17, 2020
Genetics of cystic fibrosis: Basics
C 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 perspectives
Y Fichou, C Férec
Molecular Human Reproduction
|
September 1, 1996
Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens
M 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 systems
L Raud, C Férec, Y Fichou
Blood
|
April 9, 1999
HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis
C 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 assay
B Mercier, L Burlot, C Férec
Clinical Chemistry
|
August 22, 2001
Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC
G Le Gac, C Mura, C Férec
Human Genetics
|
November 10, 2001
Molecular pathology and evolutionary and physiological implications of pancreatitis-associated cationic trypsinogen mutations
J 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 population
Y Fichou, C L Maréchal, C Férec
Clinical Genetics
|
June 24, 2010
Revealing the human mutome
J M Chen, C Férec, D N Cooper
Page
of 11
Search research articles
Search
Showing results (1-10 of 110) with videos related to
Sort By:
Page
of 11
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 17, 2020
Genetics of cystic fibrosis: Basics
C 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 perspectives
Y Fichou, C Férec
Molecular Human Reproduction
|
September 1, 1996
Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens
M 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 systems
L Raud, C Férec, Y Fichou
Blood
|
April 9, 1999
HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis
C 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 assay
B Mercier, L Burlot, C Férec
Clinical Chemistry
|
August 22, 2001
Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC
G Le Gac, C Mura, C Férec
Human Genetics
|
November 10, 2001
Molecular pathology and evolutionary and physiological implications of pancreatitis-associated cationic trypsinogen mutations
J 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 population
Y Fichou, C L Maréchal, C Férec
Clinical Genetics
|
June 24, 2010
Revealing the human mutome
J M Chen, C Férec, D N Cooper
Page
of 11