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European Journal of Medical Genetics|March 31, 2009
Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbancesMarianne Doornbos, Birgit Sikkema-Raddatz, Claudia A L Ruijvenkamp, et al.European Journal of Medical Genetics|February 15, 2014
Overlapping microdeletions involving 15q22.2 narrow the critical region for intellectual disability to NARG2 and RORAToshiyuki Yamamoto, Maria Antonietta Mencarelli, Chiara Di Marco, et al.Journal of the American Society of Nephrology : JASN|April 23, 2003
Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney diseaseRiccardo Magistroni, Ning He, Kairong Wang, et al.Journal of the American Society of Nephrology : JASN|July 10, 2010
Genetic variation of DKK3 may modify renal disease severity in ADPKDMichelle Liu, Sally Shi, Sean Senthilnathan, et al.Pageof 2