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M Claustres

Showing results (71-80 of 143) with videos related to

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American Journal of Human Genetics|November 5, 1997
CFTR gene mutations in men with bilateral ejaculatory-duct obstruction and anomalies of the seminal vesiclesD Meschede, B Dworniczak, H M Behre, et al.
Annales De Biologie Clinique|June 9, 2001
[Genetic testing for cystic fibrosis: evaluation of the Elucigene CF20 kit in blood and buccal cells]D Feldmann, C Guittard, M D Georges, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 10, 2001
[CFTR gene analyis in 207 patients with cystic fibrosis in southwest France: high frequency of N1303K and 1811+1.6bA>G mutations]S Federici, A Iron, M P Reboul, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 14, 2003
[Movement disorders in childhood: classification and genetic update]A Roubertie, F Rivier, S Tuffery-Giraud, et al.
Genomics|July 1, 1992
A new mutation (1078delT) in exon 7 of the CFTR gene in a southern French adult with cystic fibrosisM Claustres, B Gerrard, M B White, et al.
Presse Medicale (Paris, France : 1983)|January 19, 1985
[Urinary excretion of 3-methylhistidine. Value and application to the study of protein catabolism]J L Richard, M Rodier, J Bringer, et al.
Journal De Genetique Humaine|September 1, 1989
[DNA amplification in the study of polymorphisms linked to the cystic fibrosis gene]M Claustres, H Bellet, M Desgeorges, et al.
Human Mutation|January 1, 1994
A novel mutation (Val-373 to Glu) in the catalytic domain of factor IX, resulting in moderately/severe hemophilia B in a southern French patientP Aguilar-Martinez, M C Romey, J C Gris, et al.
Human Genetics|September 1, 1994
Factor IX gene mutations causing haemophilia B: comparison of SSC screening versus systematic DNA sequencing and diagnostic applicationsP Aguilar-Martinez, M C Romey, J F Schved, et al.
Human Reproduction (Oxford, England)|December 22, 1999
Complete mutational screening of the cystic fibrosis transmembrane conductance regulator gene: cystic fibrosis mutations are not involved in healthy men with reduced sperm qualityN Pallares-Ruiz, S Carles, M Des Georges, et al.
Pageof 15

Showing results (71-80 of 143) with videos related to

Sort By:
Pageof 15
American Journal of Human Genetics|November 5, 1997
CFTR gene mutations in men with bilateral ejaculatory-duct obstruction and anomalies of the seminal vesiclesD Meschede, B Dworniczak, H M Behre, et al.
Annales De Biologie Clinique|June 9, 2001
[Genetic testing for cystic fibrosis: evaluation of the Elucigene CF20 kit in blood and buccal cells]D Feldmann, C Guittard, M D Georges, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 10, 2001
[CFTR gene analyis in 207 patients with cystic fibrosis in southwest France: high frequency of N1303K and 1811+1.6bA>G mutations]S Federici, A Iron, M P Reboul, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 14, 2003
[Movement disorders in childhood: classification and genetic update]A Roubertie, F Rivier, S Tuffery-Giraud, et al.
Genomics|July 1, 1992
A new mutation (1078delT) in exon 7 of the CFTR gene in a southern French adult with cystic fibrosisM Claustres, B Gerrard, M B White, et al.
Presse Medicale (Paris, France : 1983)|January 19, 1985
[Urinary excretion of 3-methylhistidine. Value and application to the study of protein catabolism]J L Richard, M Rodier, J Bringer, et al.
Journal De Genetique Humaine|September 1, 1989
[DNA amplification in the study of polymorphisms linked to the cystic fibrosis gene]M Claustres, H Bellet, M Desgeorges, et al.
Human Mutation|January 1, 1994
A novel mutation (Val-373 to Glu) in the catalytic domain of factor IX, resulting in moderately/severe hemophilia B in a southern French patientP Aguilar-Martinez, M C Romey, J C Gris, et al.
Human Genetics|September 1, 1994
Factor IX gene mutations causing haemophilia B: comparison of SSC screening versus systematic DNA sequencing and diagnostic applicationsP Aguilar-Martinez, M C Romey, J F Schved, et al.
Human Reproduction (Oxford, England)|December 22, 1999
Complete mutational screening of the cystic fibrosis transmembrane conductance regulator gene: cystic fibrosis mutations are not involved in healthy men with reduced sperm qualityN Pallares-Ruiz, S Carles, M Des Georges, et al.
Pageof 15