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S Bevan

Showing results (231-240 of 238) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|April 9, 2014
Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3)Angela Rogers, M Andrew Nesbit, Fadil M Hannan, et al.
Blood|November 23, 2000
Linkage analysis for major histocompatibility complex-related genetic susceptibility in familial chronic lymphocytic leukemiaS Bevan, D Catovsky, E Matutes, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2016
A Follow-Up Study of the Prevalence of Valvular Heart Abnormalities in Hyperprolactinemic Patients Treated With CabergolineWilliam M Drake, Craig E Stiles, John S Bevan, et al.
Journal of Medical Genetics|May 16, 2002
Genome screening of coeliac diseaseS Popat, S Bevan, C P Braegger, et al.
American Journal of Human Genetics|April 3, 2001
Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43N A Alam, S Bevan, M Churchman, et al.
Journal of Medical Genetics|October 3, 1999
Contribution of the MHC region to the familial risk of coeliac diseaseS Bevan, S Popat, C P Braegger, et al.
Gut|April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposisK Woodford-Richens, S Bevan, M Churchman, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2014
Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohortJudit Dénes, Francesca Swords, Eleanor Rattenberry, et al.
Pageof 24

Showing results (231-240 of 238) with videos related to

Sort By:
Pageof 24
You have reached the last page of results.This site can display upto 238 results.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2014
Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3)Angela Rogers, M Andrew Nesbit, Fadil M Hannan, et al.
Blood|November 23, 2000
Linkage analysis for major histocompatibility complex-related genetic susceptibility in familial chronic lymphocytic leukemiaS Bevan, D Catovsky, E Matutes, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2016
A Follow-Up Study of the Prevalence of Valvular Heart Abnormalities in Hyperprolactinemic Patients Treated With CabergolineWilliam M Drake, Craig E Stiles, John S Bevan, et al.
Journal of Medical Genetics|May 16, 2002
Genome screening of coeliac diseaseS Popat, S Bevan, C P Braegger, et al.
American Journal of Human Genetics|April 3, 2001
Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43N A Alam, S Bevan, M Churchman, et al.
Journal of Medical Genetics|October 3, 1999
Contribution of the MHC region to the familial risk of coeliac diseaseS Bevan, S Popat, C P Braegger, et al.
Gut|April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposisK Woodford-Richens, S Bevan, M Churchman, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2014
Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohortJudit Dénes, Francesca Swords, Eleanor Rattenberry, et al.
Pageof 24