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The Journal of Clinical Endocrinology and Metabolism
|
May 1, 1986
Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein
P A Donohoue, C van Dop, R H McLean, et al.
Biochemical and Biophysical Research Communications
|
February 13, 1987
Prevalence of polymorphic 21-hydroxylase gene (CA21HB) mutations in salt-losing congenital adrenal hyperplasia
N Jospe, P A Donohoue, C Van Dop, et al.
The Journal of Pediatrics
|
July 1, 1982
Hypothyroidism in the congenital nephrotic syndrome
R H McLean, T L Kennedy, M Rosoulpour, et al.
The Journal of Pediatrics
|
January 1, 1990
Neonatal hemodialysis: effective therapy for the encephalopathy of inborn errors of metabolism
S L Rutledge, P L Havens, M W Haymond, et al.
Clinical Immunology and Immunopathology
|
September 1, 1981
C4 polymorphism and HLA linkage: studies in a family with hereditary C4 deficiency
M Ballow, R H McLean, E J Yunis, et al.
Biochemical and Biophysical Research Communications
|
April 29, 1986
Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genes
P A Donohoue, N Jospe, C J Migeon, et al.
Arthritis and Rheumatism
|
August 1, 1980
Familial discoid lupus erythematosus associated with heterozygote C2 deficiency
D C Belin, B J Bordwell, M E Einarson, et al.
Kidney International
|
February 1, 1973
Immunologic aspects of the nephrotic syndrome
A F Michael, R H McLean, L P Roy, et al.
The Journal of Biological Chemistry
|
November 4, 1994
Hemolytically inactive C4B complement allotype caused by a proline to leucine mutation in the C5-binding site
R H McLean, G Niblack, B Julian, et al.
The Journal of Rheumatology
|
June 1, 1987
Systemic sclerosis (scleroderma): clinical, genetic, and serologic subsets
J Z Livingston, T E Scott, F M Wigley, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 76) with videos related to
Sort By:
Page
of 8
The Journal of Clinical Endocrinology and Metabolism
|
May 1, 1986
Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein
P A Donohoue, C van Dop, R H McLean, et al.
Biochemical and Biophysical Research Communications
|
February 13, 1987
Prevalence of polymorphic 21-hydroxylase gene (CA21HB) mutations in salt-losing congenital adrenal hyperplasia
N Jospe, P A Donohoue, C Van Dop, et al.
The Journal of Pediatrics
|
July 1, 1982
Hypothyroidism in the congenital nephrotic syndrome
R H McLean, T L Kennedy, M Rosoulpour, et al.
The Journal of Pediatrics
|
January 1, 1990
Neonatal hemodialysis: effective therapy for the encephalopathy of inborn errors of metabolism
S L Rutledge, P L Havens, M W Haymond, et al.
Clinical Immunology and Immunopathology
|
September 1, 1981
C4 polymorphism and HLA linkage: studies in a family with hereditary C4 deficiency
M Ballow, R H McLean, E J Yunis, et al.
Biochemical and Biophysical Research Communications
|
April 29, 1986
Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genes
P A Donohoue, N Jospe, C J Migeon, et al.
Arthritis and Rheumatism
|
August 1, 1980
Familial discoid lupus erythematosus associated with heterozygote C2 deficiency
D C Belin, B J Bordwell, M E Einarson, et al.
Kidney International
|
February 1, 1973
Immunologic aspects of the nephrotic syndrome
A F Michael, R H McLean, L P Roy, et al.
The Journal of Biological Chemistry
|
November 4, 1994
Hemolytically inactive C4B complement allotype caused by a proline to leucine mutation in the C5-binding site
R H McLean, G Niblack, B Julian, et al.
The Journal of Rheumatology
|
June 1, 1987
Systemic sclerosis (scleroderma): clinical, genetic, and serologic subsets
J Z Livingston, T E Scott, F M Wigley, et al.
Page
of 8