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R H McLean

Showing results (61-70 of 76) with videos related to

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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 proteinP 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 hyperplasiaN Jospe, P A Donohoue, C Van Dop, et al.
The Journal of Pediatrics|July 1, 1982
Hypothyroidism in the congenital nephrotic syndromeR 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 metabolismS 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 deficiencyM 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 genesP A Donohoue, N Jospe, C J Migeon, et al.
Arthritis and Rheumatism|August 1, 1980
Familial discoid lupus erythematosus associated with heterozygote C2 deficiencyD C Belin, B J Bordwell, M E Einarson, et al.
Kidney International|February 1, 1973
Immunologic aspects of the nephrotic syndromeA 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 siteR H McLean, G Niblack, B Julian, et al.
The Journal of Rheumatology|June 1, 1987
Systemic sclerosis (scleroderma): clinical, genetic, and serologic subsetsJ Z Livingston, T E Scott, F M Wigley, et al.
Pageof 8

Showing results (61-70 of 76) with videos related to

Sort By:
Pageof 8
The Journal of Clinical Endocrinology and Metabolism|May 1, 1986
Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B proteinP 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 hyperplasiaN Jospe, P A Donohoue, C Van Dop, et al.
The Journal of Pediatrics|July 1, 1982
Hypothyroidism in the congenital nephrotic syndromeR 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 metabolismS 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 deficiencyM 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 genesP A Donohoue, N Jospe, C J Migeon, et al.
Arthritis and Rheumatism|August 1, 1980
Familial discoid lupus erythematosus associated with heterozygote C2 deficiencyD C Belin, B J Bordwell, M E Einarson, et al.
Kidney International|February 1, 1973
Immunologic aspects of the nephrotic syndromeA 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 siteR H McLean, G Niblack, B Julian, et al.
The Journal of Rheumatology|June 1, 1987
Systemic sclerosis (scleroderma): clinical, genetic, and serologic subsetsJ Z Livingston, T E Scott, F M Wigley, et al.
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