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Annals of Human Genetics|March 16, 2011
Investigation of the HIN200 locus in UK SLE families identifies novel copy number variantsMichelle M A Fernando, Adam J de Smith, Lachlan Coin, et al.Nature Methods|June 1, 2010
cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVsLachlan J M Coin, Julian E Asher, Robin G Walters, et al.Endocrinology and Metabolism Clinics of North America|April 25, 2006
Genetic basis of maturity-onset diabetes of the youngMartine Vaxillaire, Philippe FroguelCurrent Diabetes Reports|October 25, 2017
Disentangling the Role of Melatonin and its Receptor MTNR1B in Type 2 Diabetes: Still a Long Way to Go?Amélie Bonnefond, Philippe FroguelJournal of Diabetes|July 9, 2016
Monogenic diabetes: Implementation of translational genomic research towards precision medicineMartine Vaxillaire, Philippe FroguelMedecine Sciences : M/S|March 11, 2006
[ENPP1, the first example of common genetic link between childhood and adult obesity and type 2 diabetes]David Meyre, Philippe FroguelEndocrine Reviews|April 26, 2008
Monogenic diabetes in the young, pharmacogenetics and relevance to multifactorial forms of type 2 diabetesMartine Vaxillaire, Philippe FroguelDiabetes|October 27, 2004
Genetics of the APM1 locus and its contribution to type 2 diabetes susceptibility in French CaucasiansFernando Gibson, Philippe FroguelGenome Biology|August 1, 2013
Next-generation sequencing for identifying new genes in rare genetic diseases: many challenges and a pinch of luckAmélie Bonnefond, Philippe FroguelCurrent Diabetes Reports|May 1, 2008
TCF7L2 genetic defect and type 2 diabetesStéphane Cauchi, Philippe FroguelPageof 53