Search research articles
Contact Us
Filters
Showing results (171-180 of 188) with videos related to
Page
of 19
Sort By:
Thyroid : Official Journal of the American Thyroid Association
|
October 19, 1999
The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptor
D Tiosano, S Pannain, G Vassart, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 8, 2001
Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C
V Meiner, S Shpitzen, H Mandel, et al.
The Journal of Clinical Investigation
|
March 11, 2000
Molecular basis of variant pseudo-hurler polydystrophy (mucolipidosis IIIC)
A Raas-Rothschild, V Cormier-Daire, M Bao, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1993
Hypothalamic pituitary adrenal function in the extremely low birth weight infant
C E Hanna, L D Keith, M A Colasurdo, et al.
Chemosphere
|
December 17, 2003
Serum concentrations of perfluorooctanesulfonate and other fluorochemicals in an elderly population from Seattle, Washington
Geary W Olsen, Timothy R Church, Eric B Larson, et al.
Nucleic Acids Research
|
February 21, 2024
Pathogenic CANVAS (AAGGG)n repeats stall DNA replication due to the formation of alternative DNA structures
Julia A Hisey, Elina A Radchenko, Nicholas H Mandel, et al.
AIHA Journal : a Journal for the Science of Occupational and Environmental Health and Safety
|
October 3, 2003
An occupational exposure assessment of a perfluorooctanesulfonyl fluoride production site: biomonitoring
Geary W Olsen, Perry W Logan, Kristen J Hansen, et al.
American Journal of Human Genetics
|
April 16, 1998
The gene for glycogen-storage disease type 1b maps to chromosome 11q23
B Annabi, H Hiraiwa, B C Mansfield, et al.
Environmental Research
|
March 25, 2023
Non-asbestiform elongate mineral particles and mesothelioma risk: Human and experimental evidence
Julie E Goodman, Michael J Becich, David M Bernstein, et al.
American Journal of Human Genetics
|
November 14, 2007
Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapy
S Gobin-Limballe, F Djouadi, F Aubey, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 188) with videos related to
Sort By:
Page
of 19
Thyroid : Official Journal of the American Thyroid Association
|
October 19, 1999
The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptor
D Tiosano, S Pannain, G Vassart, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 8, 2001
Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C
V Meiner, S Shpitzen, H Mandel, et al.
The Journal of Clinical Investigation
|
March 11, 2000
Molecular basis of variant pseudo-hurler polydystrophy (mucolipidosis IIIC)
A Raas-Rothschild, V Cormier-Daire, M Bao, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1993
Hypothalamic pituitary adrenal function in the extremely low birth weight infant
C E Hanna, L D Keith, M A Colasurdo, et al.
Chemosphere
|
December 17, 2003
Serum concentrations of perfluorooctanesulfonate and other fluorochemicals in an elderly population from Seattle, Washington
Geary W Olsen, Timothy R Church, Eric B Larson, et al.
Nucleic Acids Research
|
February 21, 2024
Pathogenic CANVAS (AAGGG)n repeats stall DNA replication due to the formation of alternative DNA structures
Julia A Hisey, Elina A Radchenko, Nicholas H Mandel, et al.
AIHA Journal : a Journal for the Science of Occupational and Environmental Health and Safety
|
October 3, 2003
An occupational exposure assessment of a perfluorooctanesulfonyl fluoride production site: biomonitoring
Geary W Olsen, Perry W Logan, Kristen J Hansen, et al.
American Journal of Human Genetics
|
April 16, 1998
The gene for glycogen-storage disease type 1b maps to chromosome 11q23
B Annabi, H Hiraiwa, B C Mansfield, et al.
Environmental Research
|
March 25, 2023
Non-asbestiform elongate mineral particles and mesothelioma risk: Human and experimental evidence
Julie E Goodman, Michael J Becich, David M Bernstein, et al.
American Journal of Human Genetics
|
November 14, 2007
Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapy
S Gobin-Limballe, F Djouadi, F Aubey, et al.
Page
of 19