A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosisLEMOS, Manuel C; KOTANKO, Peter; CHRISTIE, Paul T et al.The Journal of clinical endocrinology and metabolism. 2005, Vol 90, Num 9, pp 5386-5392, issn 0021-972X, 7 p.Article

A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1LEMOS, Manuel C; HARDING, Brian; SHALET, Stephen M et al.Clinical endocrinology (Oxford. Print). 2007, Vol 66, Num 5, pp 709-713, issn 0300-0664, 5 p.Article

Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sitesHANNAN, Fadil M; NESBIT, M. Andrew; LEMOS, Manuel C et al.Human molecular genetics (Print). 2012, Vol 21, Num 12, pp 2768-2778, issn 0964-6906, 11 p.Article

MEN1 Gene Replacement Therapy Reduces Proliferation Rates in a Mouse Model of Pituitary AdenomasWALLS, Gerard V; LEMOS, Manuel C; CHRISTIE, Paul T et al.Cancer research (Chicago, Ill.). 2012, Vol 72, Num 19, pp 5060-5068, issn 0008-5472, 9 p.Article

PROP1 gene analysis in portuguese patients with combined pituitary hormone deficiencyLEMOS, Manuel C; GOMES, Leonor; CASTRO, Joao J et al.Clinical endocrinology (Oxford. Print). 2006, Vol 65, Num 4, pp 479-485, issn 0300-0664, 7 p.Article