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Human Genetics
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August 1, 1996
Linkage disequilibrium between the four most common cystic fibrosis mutations and microsatellite haplotypes in the Celtic population of Brittany
M De Braekeleer, A Chaventré, G Bertorelle, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
June 19, 2007
CFTR mutations in the Algerian population
O Loumi, C Ferec, B Mercier, et al.
Nephron
|
April 5, 2001
Inheritance of a stable mutation in a family with early-onset disease
R A Perrichot, B Mercier, L de Parscau, et al.
Journal of Medical Genetics
|
March 21, 1998
Absence of mutations in the interspecies conserved regions of the CFTR promoter region in cystic fibrosis (CF) and CF related patients
C Verlingue, S Vuillaumier, B Mercier, et al.
Journal of Pharmaceutical Sciences
|
April 11, 2000
Phosphonocationic lipids in protein delivery to mice lungs
C Guillaume, P Delépine, B Mercier, et al.
Fetal Diagnosis and Therapy
|
September 1, 1993
Prenatal diagnosis of cystic fibrosis in different European populations: application of denaturing gradient gel electrophoresis
C Férec, C Verlingue, M P Audrézet, et al.
European Journal of Applied Physiology and Occupational Physiology
|
January 1, 1997
Metabolic and hormonal responses during repeated bouts of brief and intense exercise: effects of pre-exercise glucose ingestion
D Wouassi, J Mercier, S Ahmaidi, et al.
Human Heredity
|
September 1, 1993
Identification of three novel cystic fibrosis mutations in a sample of Italian cystic fibrosis patients
M P Audrézet, G Novelli, B Mercier, et al.
Nature Genetics
|
June 1, 1992
Detection of over 98% cystic fibrosis mutations in a Celtic population
C Férec, M P Audrezet, B Mercier, et al.
Thrombosis and Haemostasis
|
July 31, 1998
Prevalence of 20210 A allele of the prothrombin gene in venous thromboembolism patients
C Leroyer, B Mercier, E Oger, et al.
Page
of 17
Search research articles
Search
Showing results (91-100 of 164) with videos related to
Sort By:
Page
of 17
Human Genetics
|
August 1, 1996
Linkage disequilibrium between the four most common cystic fibrosis mutations and microsatellite haplotypes in the Celtic population of Brittany
M De Braekeleer, A Chaventré, G Bertorelle, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
June 19, 2007
CFTR mutations in the Algerian population
O Loumi, C Ferec, B Mercier, et al.
Nephron
|
April 5, 2001
Inheritance of a stable mutation in a family with early-onset disease
R A Perrichot, B Mercier, L de Parscau, et al.
Journal of Medical Genetics
|
March 21, 1998
Absence of mutations in the interspecies conserved regions of the CFTR promoter region in cystic fibrosis (CF) and CF related patients
C Verlingue, S Vuillaumier, B Mercier, et al.
Journal of Pharmaceutical Sciences
|
April 11, 2000
Phosphonocationic lipids in protein delivery to mice lungs
C Guillaume, P Delépine, B Mercier, et al.
Fetal Diagnosis and Therapy
|
September 1, 1993
Prenatal diagnosis of cystic fibrosis in different European populations: application of denaturing gradient gel electrophoresis
C Férec, C Verlingue, M P Audrézet, et al.
European Journal of Applied Physiology and Occupational Physiology
|
January 1, 1997
Metabolic and hormonal responses during repeated bouts of brief and intense exercise: effects of pre-exercise glucose ingestion
D Wouassi, J Mercier, S Ahmaidi, et al.
Human Heredity
|
September 1, 1993
Identification of three novel cystic fibrosis mutations in a sample of Italian cystic fibrosis patients
M P Audrézet, G Novelli, B Mercier, et al.
Nature Genetics
|
June 1, 1992
Detection of over 98% cystic fibrosis mutations in a Celtic population
C Férec, M P Audrezet, B Mercier, et al.
Thrombosis and Haemostasis
|
July 31, 1998
Prevalence of 20210 A allele of the prothrombin gene in venous thromboembolism patients
C Leroyer, B Mercier, E Oger, et al.
Page
of 17