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D Learoyd

Showing results (1-10 of 9) with videos related to

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Australian and New Zealand Journal of Medicine|December 1, 1990
Medroxyprogesterone induced Cushing's syndromeD Learoyd, A McElduff
Papua and New Guinea Medical Journal|June 1, 1989
An assessment of the nutritional status of preschool children in Western Papua New Guinea, 1978 to 1986R P McNair, D Learoyd
World Journal of Surgery|February 28, 2018
Medullary Thyroid Carcinoma: Survival Analysis and Evaluation of Mutation-Specific Immunohistochemistry in Detection of Sporadic DiseaseS Jayakody, J Reagh, M Bullock, et al.
World Journal of Surgery|May 4, 2016
BRAF(V600E) Mutation is Associated with Decreased Disease-Free Survival in Papillary Thyroid CancerS Fraser, C Go, A Aniss, et al.
Bone|February 1, 2015
Mortality associated with primary hyperparathyroidismP B Clifton-Bligh, M L Nery, R Supramaniam, et al.
Journal of Medical Genetics|January 7, 2005
A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testingJ W Cardinal, L Bergman, N Hayward, et al.
Journal of Medical Genetics|March 10, 2006
Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14J V Warner, D R Nyholt, F Busfield, et al.
Journal of Medical Genetics|February 27, 2004
Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implicationsJ Warner, M Epstein, A Sweet, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumorsD J Marsh, Z Zheng, A Arnold, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Australian and New Zealand Journal of Medicine|December 1, 1990
Medroxyprogesterone induced Cushing's syndromeD Learoyd, A McElduff
Papua and New Guinea Medical Journal|June 1, 1989
An assessment of the nutritional status of preschool children in Western Papua New Guinea, 1978 to 1986R P McNair, D Learoyd
World Journal of Surgery|February 28, 2018
Medullary Thyroid Carcinoma: Survival Analysis and Evaluation of Mutation-Specific Immunohistochemistry in Detection of Sporadic DiseaseS Jayakody, J Reagh, M Bullock, et al.
World Journal of Surgery|May 4, 2016
BRAF(V600E) Mutation is Associated with Decreased Disease-Free Survival in Papillary Thyroid CancerS Fraser, C Go, A Aniss, et al.
Bone|February 1, 2015
Mortality associated with primary hyperparathyroidismP B Clifton-Bligh, M L Nery, R Supramaniam, et al.
Journal of Medical Genetics|January 7, 2005
A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testingJ W Cardinal, L Bergman, N Hayward, et al.
Journal of Medical Genetics|March 10, 2006
Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14J V Warner, D R Nyholt, F Busfield, et al.
Journal of Medical Genetics|February 27, 2004
Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implicationsJ Warner, M Epstein, A Sweet, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumorsD J Marsh, Z Zheng, A Arnold, et al.
Pageof 1