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C E Jackson

Showing results (151-160 of 180) with videos related to

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Neuroscience Letters|April 22, 2005
An autosomal genomic screen for dementia in an extended Amish familyA E Ashley-Koch, Y Shao, J B Rimmler, et al.
Oncogene|February 2, 1995
A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTCC Eng, D P Smith, L M Mulligan, et al.
Nature Genetics|December 1, 1994
Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1K A McAllister, K M Grogg, D W Johnson, et al.
Journal of Medical Genetics|December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotypeK A McAllister, F Lennon, B Bowles-Biesecker, et al.
Cancer Research|December 1, 1996
Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomasM Goggins, M Schutte, J Lu, et al.
Archives of Neurology|May 18, 1999
Chronic cryptogenic sensory polyneuropathy: clinical and laboratory characteristicsG I Wolfe, N S Baker, A A Amato, et al.
Genome Research|August 1, 1995
A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12D W Johnson, J N Berg, C J Gallione, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|April 1, 1997
Genomic sequencing of DPC4 in the analysis of familial pancreatic carcinomaC A Moskaluk, R H Hruban, M Schutte, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1996
Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domainsH Heath, S Odelberg, C E Jackson, et al.
Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.
Pageof 18

Showing results (151-160 of 180) with videos related to

Sort By:
Pageof 18
Neuroscience Letters|April 22, 2005
An autosomal genomic screen for dementia in an extended Amish familyA E Ashley-Koch, Y Shao, J B Rimmler, et al.
Oncogene|February 2, 1995
A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTCC Eng, D P Smith, L M Mulligan, et al.
Nature Genetics|December 1, 1994
Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1K A McAllister, K M Grogg, D W Johnson, et al.
Journal of Medical Genetics|December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotypeK A McAllister, F Lennon, B Bowles-Biesecker, et al.
Cancer Research|December 1, 1996
Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomasM Goggins, M Schutte, J Lu, et al.
Archives of Neurology|May 18, 1999
Chronic cryptogenic sensory polyneuropathy: clinical and laboratory characteristicsG I Wolfe, N S Baker, A A Amato, et al.
Genome Research|August 1, 1995
A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12D W Johnson, J N Berg, C J Gallione, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|April 1, 1997
Genomic sequencing of DPC4 in the analysis of familial pancreatic carcinomaC A Moskaluk, R H Hruban, M Schutte, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1996
Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domainsH Heath, S Odelberg, C E Jackson, et al.
Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.
Pageof 18