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Molecular and Cellular Probes|September 4, 1998
Absence of MEN2A- or 2B-type RET mutations in primary neuroblastoma tumour tissueA E Peaston, M L Camacho, M D Norris, et al.The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutationO Gimm, D J Marsh, S D Andrew, et al.Cancer Research|January 13, 2001
Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1pD E Benn, T Dwight, A L Richardson, et al.The Australian and New Zealand Journal of Surgery|February 1, 1995
Molecular genetics of thyroid and parathyroid neoplasiaB G RobinsonHuman Molecular Genetics|December 1, 1994
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogeneL M Mulligan, C Eng, T Attié, et al.Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|August 17, 2010
Toe syndactyly revisitedD J Marsh, D FloydThe Journal of Physiology|March 1, 1971
Micropuncture studies of the electrochemical aspects of fluid and electrolyte transport in individual seminiferous tubules, the epididymis and the vas deferens in ratsN Levine, D J MarshJournal of Neurochemistry|May 1, 1985
Proteolytic digestion patterns of "soluble" and "detergent-soluble" bovine caudate nucleus acetylcholinesterasesD J Marsh, J MassouliéPageof 22