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C E Jackson

Showing results (121-130 of 180) with videos related to

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Neurology|December 17, 1998
The wide spectrum of myofibrillar myopathy suggests a multifactorial etiology and pathogenesisA A Amato, K Kagan-Hallet, C E Jackson, et al.
Genomics|August 1, 1992
Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15K Young, T Foroud, P Williams, et al.
Human Molecular Genetics|June 1, 1994
A de novo mutation of the RET proto-oncogene in a patient with MEN 2AL M Mulligan, C Eng, C S Healey, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 1994
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2BK M Carlson, S Dou, D Chi, et al.
Surgery|October 17, 2001
Prophylactic total gastrectomy for familial gastric cancerF R Lewis, J D Mellinger, A Hayashi, et al.
American Journal of Human Genetics|February 11, 1999
Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1qM R Hobbs, A R Pole, G N Pidwirny, et al.
Oncogene|May 2, 1996
Characterization of the APC gene in sporadic gastric adenocarcinomasS M Powell, O W Cummings, J A Mullen, et al.
Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.
Genomics|January 1, 1994
Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7pA F Lewanda, M M Cohen, C E Jackson, et al.
Nature Genetics|January 1, 1994
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTCL M Mulligan, C Eng, C S Healey, et al.
Pageof 18

Showing results (121-130 of 180) with videos related to

Sort By:
Pageof 18
Neurology|December 17, 1998
The wide spectrum of myofibrillar myopathy suggests a multifactorial etiology and pathogenesisA A Amato, K Kagan-Hallet, C E Jackson, et al.
Genomics|August 1, 1992
Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15K Young, T Foroud, P Williams, et al.
Human Molecular Genetics|June 1, 1994
A de novo mutation of the RET proto-oncogene in a patient with MEN 2AL M Mulligan, C Eng, C S Healey, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 1994
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2BK M Carlson, S Dou, D Chi, et al.
Surgery|October 17, 2001
Prophylactic total gastrectomy for familial gastric cancerF R Lewis, J D Mellinger, A Hayashi, et al.
American Journal of Human Genetics|February 11, 1999
Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1qM R Hobbs, A R Pole, G N Pidwirny, et al.
Oncogene|May 2, 1996
Characterization of the APC gene in sporadic gastric adenocarcinomasS M Powell, O W Cummings, J A Mullen, et al.
Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.
Genomics|January 1, 1994
Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7pA F Lewanda, M M Cohen, C E Jackson, et al.
Nature Genetics|January 1, 1994
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTCL M Mulligan, C Eng, C S Healey, et al.
Pageof 18