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Diabetes & Metabolism|April 9, 2013
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous familyA Bonnefond, E Vaillant, J Philippe, et al.Diabetes & Metabolism|April 3, 2012
European genetic variants associated with type 2 diabetes in North African ArabsS Cauchi, I Ezzidi, Y El Achhab, et al.Diabetologia|December 11, 2012
Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetesA Bonnefond, L Yengo, J Philippe, et al.NPJ Genomic Medicine|February 27, 2025
Insights from the largest diverse ancestry sex-specific disease map for genetically predicted heightA Papadopoulou, E M Litkowski, M Graff, et al.Diabetologia|November 20, 2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypesA Albrechtsen, N Grarup, Y Li, et al.Pageof 2