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S Lyonnet

Showing results (31-40 of 223) with videos related to

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Human Heredity|May 1, 1997
1283 del A: a novel mutation in exon 8 of the cystic fibrosis geneT Bienvenu, S Bousquet, S Lyonnet, et al.
Medical Hypotheses|June 22, 2000
Improvement of cystic fibrosis using antitumoral drugs: a hypothesisL Faivre, J P Bonnefont, S Lyonnet, et al.
Journal of Medical Genetics|June 3, 2004
Estimating the age of rare disease mutations: the example of Triple-A syndromeE Genin, A Tullio-Pelet, F Begeot, et al.
American Journal of Medical Genetics|November 6, 1995
Sternal cleft: case report and review of a series of nine patientsD Héron, S Lyonnet, L Iserin, et al.
The British Journal of Dermatology|March 1, 1990
Recombinant interferon alpha 2a is effective in the treatment of discoid and subacute cutaneous lupus erythematosusJ Thivolet, J F Nicolas, J Kanitakis, et al.
Clinical Genetics|May 11, 2007
An overview of isolated and syndromic oesophageal atresiaD Geneviève, L de Pontual, J Amiel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Noonan syndrome: an enigma]J M Limal, D Bonnet, Y L Bouc, et al.
Archives of Disease in Childhood|December 24, 2002
Vagal overactivity: a risk factor of sudden infant death syndrome?T Shojaei-Brosseau, C Bonaïti-Pellie, S Lyonnet, et al.
Molecular Medicine (Cambridge, Mass.)|July 27, 2001
Functional characterization of three mutations of the endothelin B receptor gene in patients with Hirschsprung's disease: evidence for selective loss of Gi couplingS Fuchs, J Amiel, S Claudel, et al.
Advances in Nephrology From the Necker Hospital|January 16, 1999
RET proto-oncogene: role in kidney development and molecular pathologyR Salomon, T Attie, J Amiel, et al.
Pageof 23

Showing results (31-40 of 223) with videos related to

Sort By:
Pageof 23
Human Heredity|May 1, 1997
1283 del A: a novel mutation in exon 8 of the cystic fibrosis geneT Bienvenu, S Bousquet, S Lyonnet, et al.
Medical Hypotheses|June 22, 2000
Improvement of cystic fibrosis using antitumoral drugs: a hypothesisL Faivre, J P Bonnefont, S Lyonnet, et al.
Journal of Medical Genetics|June 3, 2004
Estimating the age of rare disease mutations: the example of Triple-A syndromeE Genin, A Tullio-Pelet, F Begeot, et al.
American Journal of Medical Genetics|November 6, 1995
Sternal cleft: case report and review of a series of nine patientsD Héron, S Lyonnet, L Iserin, et al.
The British Journal of Dermatology|March 1, 1990
Recombinant interferon alpha 2a is effective in the treatment of discoid and subacute cutaneous lupus erythematosusJ Thivolet, J F Nicolas, J Kanitakis, et al.
Clinical Genetics|May 11, 2007
An overview of isolated and syndromic oesophageal atresiaD Geneviève, L de Pontual, J Amiel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Noonan syndrome: an enigma]J M Limal, D Bonnet, Y L Bouc, et al.
Archives of Disease in Childhood|December 24, 2002
Vagal overactivity: a risk factor of sudden infant death syndrome?T Shojaei-Brosseau, C Bonaïti-Pellie, S Lyonnet, et al.
Molecular Medicine (Cambridge, Mass.)|July 27, 2001
Functional characterization of three mutations of the endothelin B receptor gene in patients with Hirschsprung's disease: evidence for selective loss of Gi couplingS Fuchs, J Amiel, S Claudel, et al.
Advances in Nephrology From the Necker Hospital|January 16, 1999
RET proto-oncogene: role in kidney development and molecular pathologyR Salomon, T Attie, J Amiel, et al.
Pageof 23