Browsing by Author Petillo, D

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Issue DateTitleAuthor(s)Citation
2004Germline And De Novo Mutations In The Hrpt2 Tumour Suppressor Gene In Familial Isolated Hyperparathyroidism (Fihp).Delbridge, Leigh; Richardson, Anne-Louise; Robinson, Bruce; Bauters, C; Calender, A; Carpten, J D; Cheng, J D; Ebeling, T; Forsberg, L; Hoog, A; Kahnoski, K; Larsson, C; Meyrier, A; Petillo, D; Proye, C; Salmela, P I; Teh, B T; Villablanca, A; Northern Clinical School: Surgery; Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: MedicineGermline And De Novo Mutations In The Hrpt2 Tumour Suppressor Gene In Familial Isolated Hyperparathyroidism (Fihp)., Journal of Medical Genetics 2005, vol.41,(3),2004,pp e32 - 1-e32 - 7
2003HRPT2 mutations are associated with malignancy in sporadic parathyroid tumoursDelbridge, Leigh; Howell, Viive; Marsh, Deborah; Philips, Jeanette; Robinson, Bruce; Chen, J; Dralle, H; Fleuren, G J; Gimm, Oliver; Hammje, K; Haven, C J; Hoang-Vu, C; Kahnoski, K; Khoo, S K; Krause, U; Morreau, H; Nelson, A E; Petillo, D; Teh, B T; Northern Clinical School: Surgery; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Medicine; Northern Clinical School: MedicineHRPT2 mutations are associated with malignancy in sporadic parathyroid tumours, Journal of Medical Genetics, vol.40,(9),2003,pp 657-663
2004Human Gene Mutations - Gene Symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndromeHowell, Viive; Chen, J; Delbridge, L. W.; Fleuren, G. J.; Haven, C. J.; Kahnoski, K; Khoo, S K; Petillo, D; Philips, J.; Robinson, B. G.; Teh, Bin T.; Northern Clinical School: Kolling InstituteHuman Gene Mutations - Gene Symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome, Human Genetics, vol.114,(2),2004,pp 221-224