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C E Jackson

Showing results (131-140 of 180) with videos related to

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The New England Journal of Medicine|June 23, 2001
Early gastric cancer in young, asymptomatic carriers of germ-line E-cadherin mutationsD G Huntsman, F Carneiro, F R Lewis, et al.
Nature Genetics|November 1, 1994
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2E W Jabs, X Li, A F Scott, et al.
Annals of Neurology|June 1, 1996
Alzheimer's disease and apolipoprotein E-4 allele in an Amish populationM A Pericak-Vance, C C Johnson, J B Rimmler, et al.
Neurology|September 12, 2000
Superficial peroneal nerve/peroneus brevis muscle biopsy in vasculitic neuropathyM P Collins, J R Mendell, M I Periquet, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 13, 2001
Inactivation of the E-cadherin gene in sporadic diffuse-type gastric cancerJ J Ascaño, H Frierson, C A Moskaluk, et al.
Journal of Neuroscience Research|August 15, 1996
Evidence against chronic antigen-specific T lymphocyte activation in myasthenia gravisA J Infante, P D Infante, C E Jackson, et al.
Arthritis and Rheumatism|November 1, 1970
Hereditary amyloidosisC Andrade, S Araki, W D Block, et al.
Human Molecular Genetics|March 1, 1993
Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2E Gardner, L Papi, D F Easton, et al.
Human Mutation|January 8, 2000
Novel germline p16(INK4) allele (Asp145Cys) in a family with multiple pancreatic carcinomas. Mutations in brief no. 148. OnlineC A Moskaluk, H Hruban, A Lietman, et al.
American Journal of Human Genetics|April 1, 1995
Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31J Szabó, B Heath, V M Hill, et al.
Pageof 18

Showing results (131-140 of 180) with videos related to

Sort By:
Pageof 18
The New England Journal of Medicine|June 23, 2001
Early gastric cancer in young, asymptomatic carriers of germ-line E-cadherin mutationsD G Huntsman, F Carneiro, F R Lewis, et al.
Nature Genetics|November 1, 1994
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2E W Jabs, X Li, A F Scott, et al.
Annals of Neurology|June 1, 1996
Alzheimer's disease and apolipoprotein E-4 allele in an Amish populationM A Pericak-Vance, C C Johnson, J B Rimmler, et al.
Neurology|September 12, 2000
Superficial peroneal nerve/peroneus brevis muscle biopsy in vasculitic neuropathyM P Collins, J R Mendell, M I Periquet, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 13, 2001
Inactivation of the E-cadherin gene in sporadic diffuse-type gastric cancerJ J Ascaño, H Frierson, C A Moskaluk, et al.
Journal of Neuroscience Research|August 15, 1996
Evidence against chronic antigen-specific T lymphocyte activation in myasthenia gravisA J Infante, P D Infante, C E Jackson, et al.
Arthritis and Rheumatism|November 1, 1970
Hereditary amyloidosisC Andrade, S Araki, W D Block, et al.
Human Molecular Genetics|March 1, 1993
Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2E Gardner, L Papi, D F Easton, et al.
Human Mutation|January 8, 2000
Novel germline p16(INK4) allele (Asp145Cys) in a family with multiple pancreatic carcinomas. Mutations in brief no. 148. OnlineC A Moskaluk, H Hruban, A Lietman, et al.
American Journal of Human Genetics|April 1, 1995
Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31J Szabó, B Heath, V M Hill, et al.
Pageof 18