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Henry Ford Hospital Medical Journal
|
January 1, 1984
Chromosomes in multiple endocrine neoplasia type 2 syndromes
D L Van Dyke, V R Babu, C E Jackson
Annals of Internal Medicine
|
January 1, 1974
Hypercalcemia and skeletal effects in chronic hypervitaminosis A
B Frame, C E Jackson, W A Reynolds, et al.
Neurology
|
March 17, 1999
Myofibrillar myopathy: no evidence of apoptosis by TUNEL
A 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 patients
S Mohan, R J Barohn, C E Jackson, et al.
Archives of Dermatology
|
September 1, 1975
Hairy cutaneous malformations of palms and soles. A hereditary condition
C 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 hyperparathyroidism
M 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 myxoma
J 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 angioedema
C E Jackson, L C Sweet, H Hayashi, et al.
The Biochemical Journal
|
August 1, 1985
Characterization of calcium-dependent membrane binding proteins of brain cortex
A 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 heterogeneity
W D Jin, C E Jackson, R J Desnick, et al.
Page
of 18
Search research articles
Search
Showing results (51-60 of 180) with videos related to
Sort By:
Page
of 18
Henry Ford Hospital Medical Journal
|
January 1, 1984
Chromosomes in multiple endocrine neoplasia type 2 syndromes
D L Van Dyke, V R Babu, C E Jackson
Annals of Internal Medicine
|
January 1, 1974
Hypercalcemia and skeletal effects in chronic hypervitaminosis A
B Frame, C E Jackson, W A Reynolds, et al.
Neurology
|
March 17, 1999
Myofibrillar myopathy: no evidence of apoptosis by TUNEL
A 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 patients
S Mohan, R J Barohn, C E Jackson, et al.
Archives of Dermatology
|
September 1, 1975
Hairy cutaneous malformations of palms and soles. A hereditary condition
C 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 hyperparathyroidism
M 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 myxoma
J 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 angioedema
C E Jackson, L C Sweet, H Hayashi, et al.
The Biochemical Journal
|
August 1, 1985
Characterization of calcium-dependent membrane binding proteins of brain cortex
A 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 heterogeneity
W D Jin, C E Jackson, R J Desnick, et al.
Page
of 18