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The New England Journal of Medicine
|
April 17, 1986
Complete suppression of the symptoms of congenital erythropoietic porphyria by long-term treatment with high-level transfusions
S Piomelli, M B Poh-Fitzpatrick, C Seaman, et al.
Annals of the New York Academy of Sciences
|
January 1, 1986
The genetic aspects of neurofibromatosis
J C Carey, B J Baty, J P Johnson, et al.
Transactions of the Association of American Physicians
|
January 1, 1978
Inheritance of hemochromatosis: linkage to HLA
G E Cartwright, M Skolnick, D B Amos, et al.
American Journal of Clinical Pathology
|
February 1, 1991
Cytologic identification of clinically occult proliferative breast disease in women with a family history of breast cancer
C J Marshall, G B Schumann, J H Ward, et al.
American Journal of Surgery
|
October 1, 1974
Cancer of the head and neck in Utah
C R Smart, J L Lyon, M Skolnick, et al.
The Pharmacogenomics Journal
|
April 8, 2004
Genetic polymorphisms of the beta-adrenergic system: association with essential hypertension and response to beta-blockade
F Filigheddu, J E Reid, C Troffa, et al.
The New England Journal of Medicine
|
July 26, 1979
Hereditary hemochromatosis. Phenotypic expression of the disease
G E Cartwright, C Q Edwards, K Kravitz, et al.
Proteins
|
January 1, 1987
Detection of human somatic cell structural gene mutations by two-dimensional electrophoresis
S M Hanash, E H Chu, R Kuick, et al.
American Journal of Human Genetics
|
February 1, 1988
Mapping of Alport syndrome to the long arm of the X chromosome
C L Atkin, S J Hasstedt, L Menlove, et al.
American Journal of Medical Genetics
|
December 1, 1983
The inheritance of immunoglobulin E: genetic linkage analysis
D A Meyers, S J Hasstedt, D G Marsh, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 51) with videos related to
Sort By:
Page
of 6
The New England Journal of Medicine
|
April 17, 1986
Complete suppression of the symptoms of congenital erythropoietic porphyria by long-term treatment with high-level transfusions
S Piomelli, M B Poh-Fitzpatrick, C Seaman, et al.
Annals of the New York Academy of Sciences
|
January 1, 1986
The genetic aspects of neurofibromatosis
J C Carey, B J Baty, J P Johnson, et al.
Transactions of the Association of American Physicians
|
January 1, 1978
Inheritance of hemochromatosis: linkage to HLA
G E Cartwright, M Skolnick, D B Amos, et al.
American Journal of Clinical Pathology
|
February 1, 1991
Cytologic identification of clinically occult proliferative breast disease in women with a family history of breast cancer
C J Marshall, G B Schumann, J H Ward, et al.
American Journal of Surgery
|
October 1, 1974
Cancer of the head and neck in Utah
C R Smart, J L Lyon, M Skolnick, et al.
The Pharmacogenomics Journal
|
April 8, 2004
Genetic polymorphisms of the beta-adrenergic system: association with essential hypertension and response to beta-blockade
F Filigheddu, J E Reid, C Troffa, et al.
The New England Journal of Medicine
|
July 26, 1979
Hereditary hemochromatosis. Phenotypic expression of the disease
G E Cartwright, C Q Edwards, K Kravitz, et al.
Proteins
|
January 1, 1987
Detection of human somatic cell structural gene mutations by two-dimensional electrophoresis
S M Hanash, E H Chu, R Kuick, et al.
American Journal of Human Genetics
|
February 1, 1988
Mapping of Alport syndrome to the long arm of the X chromosome
C L Atkin, S J Hasstedt, L Menlove, et al.
American Journal of Medical Genetics
|
December 1, 1983
The inheritance of immunoglobulin E: genetic linkage analysis
D A Meyers, S J Hasstedt, D G Marsh, et al.
Page
of 6