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The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomasO Gimm, H Chi, P L Dahia, et al.
Journal of Medical Genetics|November 1, 1995
Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytomaP A Crossey, C Eng, M Ginalska-Malinowska, et al.
American Journal of Medical Genetics|March 17, 1999
Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS)L R Otto, R L Boriack, D J Marsh, et al.
Cancer Research|May 1, 1996
Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinomaC Eng, L M Mulligan, C S Healey, et al.
Human Molecular Genetics|February 13, 2001
Transient ectopic expression of PTEN in thyroid cancer cell lines induces cell cycle arrest and cell type-dependent cell deathL P Weng, O Gimm, J B Kum, et al.
British Journal of Cancer|March 17, 2012
Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancerC R Garrett, H M Hassabo, N A Bhadkamkar, et al.
Nature Genetics|April 1, 1996
Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)P Edery, T Attié, J Amiel, et al.
Circulation|August 1, 1982
Coronary collateral function during exerciseC Eng, R E Patterson, S F Horowitz, et al.
Neoplasia (New York, N.Y.)|August 9, 2001
Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatographyD J Marsh, G Theodosopoulos, V Howell, et al.
American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses|July 3, 2018
Correlation Between mMINDS and CIWA-Ar Scoring Tools in Patients With Alcohol Withdrawal SyndromeAudrey J Littlefield, Mojdeh S Heavner, Claire C Eng, et al.
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