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C E Jackson

Showing results (51-60 of 180) with videos related to

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Henry Ford Hospital Medical Journal|January 1, 1984
Chromosomes in multiple endocrine neoplasia type 2 syndromesD L Van Dyke, V R Babu, C E Jackson
Annals of Internal Medicine|January 1, 1974
Hypercalcemia and skeletal effects in chronic hypervitaminosis AB Frame, C E Jackson, W A Reynolds, et al.
Neurology|March 17, 1999
Myofibrillar myopathy: no evidence of apoptosis by TUNELA A Amato, C E Jackson, S Lampkin, et al.
Clinical Immunology and Immunopathology|March 1, 1994
Evaluation of myosin-reactive antibodies from a panel of myasthenia gravis patientsS Mohan, R J Barohn, C E Jackson, et al.
Archives of Dermatology|September 1, 1975
Hairy cutaneous malformations of palms and soles. A hereditary conditionC E Jackson, Q C Callies, E A Krull, et al.
Archives of Surgery (Chicago, Ill. : 1960)|December 1, 1974
The extent of operation for primary hyperparathyroidismM A Block, B Frame, C E Jackson, et al.
QJM : Monthly Journal of the Association of Physicians|December 23, 2008
Histologically benign but clinically malignant: an unusual case of recurrent atrial myxomaJ R Dalzell, C E Jackson, D Castagno, et al.
The Journal of Allergy and Clinical Immunology|May 1, 1978
Evidence for nonlikage of genes for HLA and hereditary angioedemaC E Jackson, L C Sweet, H Hayashi, et al.
The Biochemical Journal|August 1, 1985
Characterization of calcium-dependent membrane binding proteins of brain cortexA R Rhoads, M Lulla, P B Moore, et al.
American Journal of Human Genetics|April 1, 1992
Mucopolysaccharidosis type VI: identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic heterogeneityW D Jin, C E Jackson, R J Desnick, et al.
Pageof 18

Showing results (51-60 of 180) with videos related to

Sort By:
Pageof 18
Henry Ford Hospital Medical Journal|January 1, 1984
Chromosomes in multiple endocrine neoplasia type 2 syndromesD L Van Dyke, V R Babu, C E Jackson
Annals of Internal Medicine|January 1, 1974
Hypercalcemia and skeletal effects in chronic hypervitaminosis AB Frame, C E Jackson, W A Reynolds, et al.
Neurology|March 17, 1999
Myofibrillar myopathy: no evidence of apoptosis by TUNELA A Amato, C E Jackson, S Lampkin, et al.
Clinical Immunology and Immunopathology|March 1, 1994
Evaluation of myosin-reactive antibodies from a panel of myasthenia gravis patientsS Mohan, R J Barohn, C E Jackson, et al.
Archives of Dermatology|September 1, 1975
Hairy cutaneous malformations of palms and soles. A hereditary conditionC E Jackson, Q C Callies, E A Krull, et al.
Archives of Surgery (Chicago, Ill. : 1960)|December 1, 1974
The extent of operation for primary hyperparathyroidismM A Block, B Frame, C E Jackson, et al.
QJM : Monthly Journal of the Association of Physicians|December 23, 2008
Histologically benign but clinically malignant: an unusual case of recurrent atrial myxomaJ R Dalzell, C E Jackson, D Castagno, et al.
The Journal of Allergy and Clinical Immunology|May 1, 1978
Evidence for nonlikage of genes for HLA and hereditary angioedemaC E Jackson, L C Sweet, H Hayashi, et al.
The Biochemical Journal|August 1, 1985
Characterization of calcium-dependent membrane binding proteins of brain cortexA R Rhoads, M Lulla, P B Moore, et al.
American Journal of Human Genetics|April 1, 1992
Mucopolysaccharidosis type VI: identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic heterogeneityW D Jin, C E Jackson, R J Desnick, et al.
Pageof 18