Search research articles
Contact Us
Filters
Showing results (231-240 of 238) with videos related to
Page
of 24
Sort By:
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 leukemia
S 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 Cabergoline
William M Drake, Craig E Stiles, John S Bevan, et al.
Journal of Medical Genetics
|
May 16, 2002
Genome screening of coeliac disease
S 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-q43
N 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 disease
S Bevan, S Popat, C P Braegger, et al.
Gut
|
April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposis
K 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 cohort
Judit Dénes, Francesca Swords, Eleanor Rattenberry, et al.
Page
of 24
Search research articles
Search
Showing results (231-240 of 238) with videos related to
Sort By:
Page
of 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 leukemia
S 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 Cabergoline
William M Drake, Craig E Stiles, John S Bevan, et al.
Journal of Medical Genetics
|
May 16, 2002
Genome screening of coeliac disease
S 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-q43
N 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 disease
S Bevan, S Popat, C P Braegger, et al.
Gut
|
April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposis
K 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 cohort
Judit Dénes, Francesca Swords, Eleanor Rattenberry, et al.
Page
of 24