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C E Jackson

Showing results (81-90 of 180) with videos related to

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The Journal of Pediatrics|June 1, 1976
Craniosynostosis, midfacial hypoplasia and foot abnormalities: an autosomal dominant phenotype in a large Amish kindredC E Jackson, L Weiss, W A Reynolds, et al.
Birth Defects Original Article Series|June 1, 1971
Classification of albinism in manC J Witkop, J G White, W E Nance, et al.
Muscle & Nerve|June 1, 1994
Prolonged paralysis due to nondepolarizing neuromuscular blocking agents and corticosteroidsR J Barohn, C E Jackson, S J Rogers, et al.
Archives of Surgery (Chicago, Ill. : 1960)|February 1, 1980
Clinical characteristics distinguishing hereditary from sporadic medullary thyroid carcinoma. Treatment implicationsM A Block, C E Jackson, K A Greenawald, et al.
Surgery|November 1, 1982
Pheochromocytoma in multiple endocrine neoplasia type II: an example of the two-hit theory of neoplasiaJ C Cerny, C E Jackson, G B Talpos, et al.
Human Heredity|January 1, 1976
Linkage relations of the loci for Kell and phenylthiocarbamide taste sensitivityP M Conneally, M Dumont-Driscoll, R S Huntzinger, et al.
American Journal of Human Genetics|December 1, 1990
The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10N L Carson, J S Wu, C E Jackson, et al.
Henry Ford Hospital Medical Journal|January 1, 1981
Combining provocative agents of calcitonin to detect medullary carcinoma of the thyroidJ C Sisson, M D Gross, J E Frietas, et al.
Henry Ford Hospital Medical Journal|January 1, 1987
Clinical value of calcitonin and carcinoembryonic antigen doubling times in medullary thyroid carcinomaC E Jackson, R A Norum, G B Talpos, et al.
Clinical Chemistry|October 1, 1982
A reagent strip for measuring the specific gravity of urineA E Burkhardt, K G Johnston, C E Waszak, et al.
Pageof 18

Showing results (81-90 of 180) with videos related to

Sort By:
Pageof 18
The Journal of Pediatrics|June 1, 1976
Craniosynostosis, midfacial hypoplasia and foot abnormalities: an autosomal dominant phenotype in a large Amish kindredC E Jackson, L Weiss, W A Reynolds, et al.
Birth Defects Original Article Series|June 1, 1971
Classification of albinism in manC J Witkop, J G White, W E Nance, et al.
Muscle & Nerve|June 1, 1994
Prolonged paralysis due to nondepolarizing neuromuscular blocking agents and corticosteroidsR J Barohn, C E Jackson, S J Rogers, et al.
Archives of Surgery (Chicago, Ill. : 1960)|February 1, 1980
Clinical characteristics distinguishing hereditary from sporadic medullary thyroid carcinoma. Treatment implicationsM A Block, C E Jackson, K A Greenawald, et al.
Surgery|November 1, 1982
Pheochromocytoma in multiple endocrine neoplasia type II: an example of the two-hit theory of neoplasiaJ C Cerny, C E Jackson, G B Talpos, et al.
Human Heredity|January 1, 1976
Linkage relations of the loci for Kell and phenylthiocarbamide taste sensitivityP M Conneally, M Dumont-Driscoll, R S Huntzinger, et al.
American Journal of Human Genetics|December 1, 1990
The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10N L Carson, J S Wu, C E Jackson, et al.
Henry Ford Hospital Medical Journal|January 1, 1981
Combining provocative agents of calcitonin to detect medullary carcinoma of the thyroidJ C Sisson, M D Gross, J E Frietas, et al.
Henry Ford Hospital Medical Journal|January 1, 1987
Clinical value of calcitonin and carcinoembryonic antigen doubling times in medullary thyroid carcinomaC E Jackson, R A Norum, G B Talpos, et al.
Clinical Chemistry|October 1, 1982
A reagent strip for measuring the specific gravity of urineA E Burkhardt, K G Johnston, C E Waszak, et al.
Pageof 18