Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism
A. A. J. Pannett(Hammersmith Hospital), Rajesh V. Thakker(Queen Mary University of London), Luisella Cianferotti(University of Florence), Brian Shine(John Radcliffe Hospital), S. A. Forbes(Hammersmith Hospital), Ann Kennedy(Nuffield Orthopaedic Centre), J. H. Duncan Bassett(Hammersmith Hospital), Branca Cavaco(Hammersmith Hospital), Brian Harding(Hammersmith Hospital), J Turner(Nuffield Orthopaedic Centre), Frances Flinter(Guy's and St Thomas' NHS Foundation Trust), C.G.H. Maidment(Wexham Park Hospital), Richard C. Trembath(King's College London)
Cited by 78
Related Papers
Gastroenteropancreatic neuroendocrine tumours
|The Lancet Oncology|2008|1.8k
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases
|Nature|1993|1.5k
New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey
|Journal of Medical Genetics|1999|971
X-linked Alport Syndrome
|Journal of the American Society of Nephrology|2000|592