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C E Jackson

Showing results (111-120 of 180) with videos related to

Pageof 18
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Neurology|February 20, 1999
Distal myasthenia gravisS P Nations, G I Wolfe, A A Amato, et al.
Medicine|January 1, 1993
Primary systemic amyloidosis: a review and an experimental, genetic, and clinical study of 29 cases with particular emphasis on the familial form. 1956J G Rukavina, W D Block, C E Jackson, et al.
The Journal of Pediatrics|December 1, 1982
Age-related probability of development of hereditary medullary thyroid carcinomaR F Gagel, C E Jackson, M A Block, et al.
American Journal of Human Genetics|May 1, 1978
Phenylketonuria heterozygote detection in families with affected childrenT D Paul, I K Brandt, L J Elsas, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mappingS Pannain, R E Weiss, C E Jackson, et al.
American Journal of Human Genetics|June 1, 1991
Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinismL B Giebel, R K Tripathi, K M Strunk, et al.
Annals of Neurology|October 1, 1996
Inclusion body myositis: clinical and pathological boundariesA A Amato, G S Gronseth, C E Jackson, et al.
Surgery|December 1, 1990
Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndromeC E Jackson, R A Norum, S B Boyd, et al.
Neurology|January 1, 1997
Evaluation of neuromuscular symptoms in veterans of the Persian Gulf WarA A Amato, A McVey, C Cha, et al.
The New England Journal of Medicine|August 30, 1973
C-cell hyperplasia preceding medullary thyroid carcinomaH J Wolfe, K E Melvin, S J Cervi-Skinner, et al.
Pageof 18

Showing results (111-120 of 180) with videos related to

Sort By:
Pageof 18
Neurology|February 20, 1999
Distal myasthenia gravisS P Nations, G I Wolfe, A A Amato, et al.
Medicine|January 1, 1993
Primary systemic amyloidosis: a review and an experimental, genetic, and clinical study of 29 cases with particular emphasis on the familial form. 1956J G Rukavina, W D Block, C E Jackson, et al.
The Journal of Pediatrics|December 1, 1982
Age-related probability of development of hereditary medullary thyroid carcinomaR F Gagel, C E Jackson, M A Block, et al.
American Journal of Human Genetics|May 1, 1978
Phenylketonuria heterozygote detection in families with affected childrenT D Paul, I K Brandt, L J Elsas, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mappingS Pannain, R E Weiss, C E Jackson, et al.
American Journal of Human Genetics|June 1, 1991
Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinismL B Giebel, R K Tripathi, K M Strunk, et al.
Annals of Neurology|October 1, 1996
Inclusion body myositis: clinical and pathological boundariesA A Amato, G S Gronseth, C E Jackson, et al.
Surgery|December 1, 1990
Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndromeC E Jackson, R A Norum, S B Boyd, et al.
Neurology|January 1, 1997
Evaluation of neuromuscular symptoms in veterans of the Persian Gulf WarA A Amato, A McVey, C Cha, et al.
The New England Journal of Medicine|August 30, 1973
C-cell hyperplasia preceding medullary thyroid carcinomaH J Wolfe, K E Melvin, S J Cervi-Skinner, et al.
Pageof 18