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P Froguel

Showing results (51-60 of 225) with videos related to

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Cytogenetic and Genome Research|November 12, 2003
Dissection of an inverted X(p21.3q27.1) chromosome associated with mental retardationF Leprêtre, V Delannoy, P Froguel, et al.
Cytogenetics and Cell Genetics|February 22, 2002
Molecular and cytogenetic characterisation of a small interstitial de novo 20p13-->p12.3 deletion in a patient with severe growth deficitF Leprêtre, C Montpellier, V Delannoy, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 13, 2007
[Neonatal diabetes: a disease linked to multiple mechanisms]I Flechtner, M Vaxillaire, H Cavé, et al.
Diabetologia|February 24, 2001
Genetic and environmental nature of the insulin resistance syndrome in Indo-Mauritian subjects with premature coronary heart disease: contribution of beta3-adrenoreceptor gene polymorphism and beta blockers on triglyceride and HDL concentrationsM Manraj, S Francke, A Hébé, et al.
Diabetes|February 1, 1989
In vitro and in vivo stability of electrode potentials in needle-type glucose sensors. Influence of needle materialG Velho, P Froguel, R Sternberg, et al.
Journees Annuelles De Diabetologie De L'Hotel-Dieu|January 1, 1997
[Leptin and genetics of obesity]K Clément, P Froguel, J Hager, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 24, 2004
The adiponectin gene SNP+45 is associated with coronary artery disease in Type 2 (non-insulin-dependent) diabetes mellitusC Lacquemant, P Froguel, S Lobbens, et al.
Diabetologia|March 27, 2002
Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in FranceM Vaxillaire, C Samson, H Cavé, et al.
Human Mutation|January 29, 2000
Big Dye terminator cycle sequencing chemistry: accuracy of the dilution process and application for screening mutations in the TCF1 and GCK genesP Boutin, C Wahl, C Samson, et al.
Cytogenetic and Genome Research|March 17, 2009
Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for diseaseA J de Smith, R G Walters, P Froguel, et al.
Pageof 23

Showing results (51-60 of 225) with videos related to

Sort By:
Pageof 23
Cytogenetic and Genome Research|November 12, 2003
Dissection of an inverted X(p21.3q27.1) chromosome associated with mental retardationF Leprêtre, V Delannoy, P Froguel, et al.
Cytogenetics and Cell Genetics|February 22, 2002
Molecular and cytogenetic characterisation of a small interstitial de novo 20p13-->p12.3 deletion in a patient with severe growth deficitF Leprêtre, C Montpellier, V Delannoy, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 13, 2007
[Neonatal diabetes: a disease linked to multiple mechanisms]I Flechtner, M Vaxillaire, H Cavé, et al.
Diabetologia|February 24, 2001
Genetic and environmental nature of the insulin resistance syndrome in Indo-Mauritian subjects with premature coronary heart disease: contribution of beta3-adrenoreceptor gene polymorphism and beta blockers on triglyceride and HDL concentrationsM Manraj, S Francke, A Hébé, et al.
Diabetes|February 1, 1989
In vitro and in vivo stability of electrode potentials in needle-type glucose sensors. Influence of needle materialG Velho, P Froguel, R Sternberg, et al.
Journees Annuelles De Diabetologie De L'Hotel-Dieu|January 1, 1997
[Leptin and genetics of obesity]K Clément, P Froguel, J Hager, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 24, 2004
The adiponectin gene SNP+45 is associated with coronary artery disease in Type 2 (non-insulin-dependent) diabetes mellitusC Lacquemant, P Froguel, S Lobbens, et al.
Diabetologia|March 27, 2002
Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in FranceM Vaxillaire, C Samson, H Cavé, et al.
Human Mutation|January 29, 2000
Big Dye terminator cycle sequencing chemistry: accuracy of the dilution process and application for screening mutations in the TCF1 and GCK genesP Boutin, C Wahl, C Samson, et al.
Cytogenetic and Genome Research|March 17, 2009
Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for diseaseA J de Smith, R G Walters, P Froguel, et al.
Pageof 23