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The Journal of Clinical Endocrinology and Metabolism
|
April 12, 2001
Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas
O Gimm, H Chi, P L Dahia, et al.
Journal of Medical Genetics
|
November 1, 1995
Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma
P A Crossey, C Eng, M Ginalska-Malinowska, et al.
Annals of Internal Medicine
|
October 15, 1992
The association between the myelodysplastic syndromes and Crohn disease
C Eng, F A Farraye, L N Shulman, et al.
American Journal of Medical Genetics
|
March 17, 1999
Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS)
L R Otto, R L Boriack, D J Marsh, et al.
Human Molecular Genetics
|
August 1, 1994
A 7 bp deletion of the RET proto-oncogene in familial Hirschsprung's disease
T Attie, A Pelet, P Sarda, et al.
Cancer Research
|
May 1, 1996
Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma
C Eng, L M Mulligan, C S Healey, et al.
Human Molecular Genetics
|
February 13, 2001
Transient ectopic expression of PTEN in thyroid cancer cell lines induces cell cycle arrest and cell type-dependent cell death
L P Weng, O Gimm, J B Kum, et al.
British Journal of Cancer
|
March 17, 2012
Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancer
C R Garrett, H M Hassabo, N A Bhadkamkar, et al.
Nature Genetics
|
April 1, 1996
Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)
P Edery, T Attié, J Amiel, et al.
Circulation
|
August 1, 1982
Coronary collateral function during exercise
C Eng, R E Patterson, S F Horowitz, et al.
Page
of 39
Search research articles
Search
Showing results (241-250 of 385) with videos related to
Sort By:
Page
of 39
The Journal of Clinical Endocrinology and Metabolism
|
April 12, 2001
Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas
O Gimm, H Chi, P L Dahia, et al.
Journal of Medical Genetics
|
November 1, 1995
Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma
P A Crossey, C Eng, M Ginalska-Malinowska, et al.
Annals of Internal Medicine
|
October 15, 1992
The association between the myelodysplastic syndromes and Crohn disease
C Eng, F A Farraye, L N Shulman, et al.
American Journal of Medical Genetics
|
March 17, 1999
Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS)
L R Otto, R L Boriack, D J Marsh, et al.
Human Molecular Genetics
|
August 1, 1994
A 7 bp deletion of the RET proto-oncogene in familial Hirschsprung's disease
T Attie, A Pelet, P Sarda, et al.
Cancer Research
|
May 1, 1996
Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma
C Eng, L M Mulligan, C S Healey, et al.
Human Molecular Genetics
|
February 13, 2001
Transient ectopic expression of PTEN in thyroid cancer cell lines induces cell cycle arrest and cell type-dependent cell death
L P Weng, O Gimm, J B Kum, et al.
British Journal of Cancer
|
March 17, 2012
Survival advantage observed with the use of metformin in patients with type II diabetes and colorectal cancer
C R Garrett, H M Hassabo, N A Bhadkamkar, et al.
Nature Genetics
|
April 1, 1996
Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)
P Edery, T Attié, J Amiel, et al.
Circulation
|
August 1, 1982
Coronary collateral function during exercise
C Eng, R E Patterson, S F Horowitz, et al.
Page
of 39