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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 17, 2020
Genetics of cystic fibrosis: Basics
C Férec, V Scotet
Molecular Genetics and Metabolism
|
September 26, 2000
Definition of a "functional R domain" of the cystic fibrosis transmembrane conductance regulator
J M Chen, V Scotet, C Ferec
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 12, 2012
[Genetics and modifier genes, atypical and rare forms]
C Férec, V Scotet, J Beucher, et al.
Pathologie-Biologie
|
January 5, 2002
[Neonatal screening for cystic fibrosis]
V Scotet, M P Audrézet, M de Braekeleer, et al.
Journal of Medical Genetics
|
June 19, 2002
Relationship between genotype and phenotype for the CFTR gene W846X mutation
I Duguépéroux, G Bellis, C Férec, et al.
British Journal of Haematology
|
May 19, 2004
Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent
G Le Gac, F Mons, S Jacolot, et al.
Journal of Medical Genetics
|
September 22, 2001
Variation of iron loading expression in C282Y homozygous haemochromatosis probands and sib pairs
C Mura, G Le Gac, V Scotet, et al.
Clinical Genetics
|
July 19, 2002
Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection system
J Andrieux, M P Audrézet, I Frachon, et al.
European Journal of Epidemiology
|
August 26, 2000
Intake of flavonoids and risk of dementia
D Commenges, V Scotet, S Renaud, et al.
Osteoarthritis and Cartilage
|
April 4, 2009
Do HOXB9 and COL1A1 genes play a role in congenital dislocation of the hip? Study in a Caucasian population
K Rouault, V Scotet, S Autret, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 17, 2020
Genetics of cystic fibrosis: Basics
C Férec, V Scotet
Molecular Genetics and Metabolism
|
September 26, 2000
Definition of a "functional R domain" of the cystic fibrosis transmembrane conductance regulator
J M Chen, V Scotet, C Ferec
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 12, 2012
[Genetics and modifier genes, atypical and rare forms]
C Férec, V Scotet, J Beucher, et al.
Pathologie-Biologie
|
January 5, 2002
[Neonatal screening for cystic fibrosis]
V Scotet, M P Audrézet, M de Braekeleer, et al.
Journal of Medical Genetics
|
June 19, 2002
Relationship between genotype and phenotype for the CFTR gene W846X mutation
I Duguépéroux, G Bellis, C Férec, et al.
British Journal of Haematology
|
May 19, 2004
Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent
G Le Gac, F Mons, S Jacolot, et al.
Journal of Medical Genetics
|
September 22, 2001
Variation of iron loading expression in C282Y homozygous haemochromatosis probands and sib pairs
C Mura, G Le Gac, V Scotet, et al.
Clinical Genetics
|
July 19, 2002
Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection system
J Andrieux, M P Audrézet, I Frachon, et al.
European Journal of Epidemiology
|
August 26, 2000
Intake of flavonoids and risk of dementia
D Commenges, V Scotet, S Renaud, et al.
Osteoarthritis and Cartilage
|
April 4, 2009
Do HOXB9 and COL1A1 genes play a role in congenital dislocation of the hip? Study in a Caucasian population
K Rouault, V Scotet, S Autret, et al.
Page
of 2