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Journal of Medical Genetics|June 1, 1994
Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?C Eng, V Murday, S Seal, et al.JAMA|October 11, 1995
Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type IIH P Neumann, C Eng, L M Mulligan, et al.Journal of Medical Genetics|August 3, 2000
RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung diseaseS Borrego, A Ruiz, M E Saez, et al.Clinical Endocrinology|March 1, 1996
Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomaD J Marsh, D L Learoyd, S D Andrew, et al.BJS Open|April 9, 2019
Evolving indications and long-term oncological outcomes of risk-reducing bilateral nipple-sparing mastectomyS R Grobmyer, H J Pederson, S A Valente, et al.Journal of the National Cancer Institute|June 8, 2000
Altered PTEN expression as a diagnostic marker for the earliest endometrial precancersG L Mutter, M C Lin, J T Fitzgerald, et al.Oncogene|May 10, 2000
Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumoursJ J Yeh, K L Lunetta, N J van Orsouw, et al.Lancet (London, England)|April 27, 2001
Germline SDHD mutation in familial phaeochromocytomaD Astuti, F Douglas, T W Lennard, et al.American Journal of Human Genetics|June 19, 2001
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paragangliomaD Astuti, F Latif, A Dallol, et al.Clinical Endocrinology|July 1, 1995
Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinomaC Eng, L M Mulligan, D P Smith, et al.Pageof 33