Andrea Villablanca
Department of Molecular Medicine
Karolinska Hospital
Stockholm
Sweden
Name/email consistency: high
- Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP). Villablanca, A., Calender, A., Forsberg, L., Höög, A., Cheng, J.D., Petillo, D., Bauters, C., Kahnoski, K., Ebeling, T., Salmela, P., Richardson, A.L., Delbridge, L., Meyrier, A., Proye, C., Carpten, J.D., Teh, B.T., Robinson, B.G., Larsson, C. J. Med. Genet. (2004)
- Genetic and clinical characterization of sporadic cystic parathyroid tumours. Villablanca, A., Farnebo, F., Teh, B.T., Farnebo, L.O., Höög, A., Larsson, C. Clin. Endocrinol. (Oxf) (2002)
- Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism. Villablanca, A., Wassif, W.S., Smith, T., Höög, A., Vierimaa, O., Kassem, M., Dwight, T., Forsberg, L., Du, Q., Learoyd, D., Jones, K., Stranks, S., Juhlin, C., Teh, B.T., Carling, T., Robinson, B., Larsson, C. Eur. J. Endocrinol. (2002)
