McLean RH - Search Results

1

Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein.

Donohoue PA, van Dop C, McLean RH, White PC, Jospe N, Migeon CJ. Donohoue PA, et al. Among authors: mclean rh. J Clin Endocrinol Metab. 1986 May;62(5):995-1002. doi: 10.1210/jcem-62-5-995. J Clin Endocrinol Metab. 1986. PMID: 3007562

2

Coupling of HLA-A3,Cw6,Bw47,DR7 and a normal CA21HB steroid 21-hydroxylase gene in the Old Order Amish.

Donohoue PA, Van Dop C, Migeon CJ, McLean RH, Bias WB. Donohoue PA, et al. Among authors: mclean rh. J Clin Endocrinol Metab. 1987 Nov;65(5):980-6. doi: 10.1210/jcem-65-5-980. J Clin Endocrinol Metab. 1987. PMID: 2822757

3

Prevalence of polymorphic 21-hydroxylase gene (CA21HB) mutations in salt-losing congenital adrenal hyperplasia.

Jospe N, Donohoue PA, Van Dop C, McLean RH, Bias WB, Migeon CJ. Jospe N, et al. Among authors: mclean rh. Biochem Biophys Res Commun. 1987 Feb 13;142(3):798-804. doi: 10.1016/0006-291x(87)91484-7. Biochem Biophys Res Commun. 1987. PMID: 3030300 Free article.

4

Restriction fragment analysis of duplication of the fourth component of complement (C4A).

McLean RH, Donohoue PA, Jospe N, Bias WB, Van Dop C, Migeon CJ. McLean RH, et al. Genomics. 1988 Jan;2(1):76-85. doi: 10.1016/0888-7543(88)90111-5. Genomics. 1988. PMID: 2838414

5

Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genes.

Donohoue PA, Jospe N, Migeon CJ, McLean RH, Bias WB, White PC, Van Dop C. Donohoue PA, et al. Among authors: mclean rh. Biochem Biophys Res Commun. 1986 Apr 29;136(2):722-9. doi: 10.1016/0006-291x(86)90499-7. Biochem Biophys Res Commun. 1986. PMID: 3010994 Free article.

6

A unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotype.

Fasano MB, Winkelstein JA, LaRosa T, Bias WB, McLean RH. Fasano MB, et al. Among authors: mclean rh. J Clin Invest. 1992 Oct;90(4):1180-4. doi: 10.1172/JCI115978. J Clin Invest. 1992. PMID: 1401055 Free PMC article.

7

Molecular heterogeneity of complement component C4-null and 21-hydroxylase genes in systemic lupus erythematosus.

Goldstein R, Arnett FC, McLean RH, Bias WB, Duvic M. Goldstein R, et al. Among authors: mclean rh. Arthritis Rheum. 1988 Jun;31(6):736-44. doi: 10.1002/art.1780310606. Arthritis Rheum. 1988. PMID: 3260100

8

Hypomorphic C4B* 15 variant of the fourth component of complement.

Christenson MJ, LaRosa T, Jung M, Bias WB, McLean RH. Christenson MJ, et al. Among authors: mclean rh. FEBS Lett. 1990 Jan 29;260(2):183-6. doi: 10.1016/0014-5793(90)80099-5. FEBS Lett. 1990. PMID: 1688812 Free article.

9

Association of homozygous C4B deficiency with bacterial meningitis.

Rowe PC, McLean RH, Wood RA, Leggiadro RJ, Winkelstein JA. Rowe PC, et al. Among authors: mclean rh. J Infect Dis. 1989 Sep;160(3):448-51. doi: 10.1093/infdis/160.3.448. J Infect Dis. 1989. PMID: 2788199

10

Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura.

McLean RH, Wyatt RJ, Julian BA. McLean RH, et al. Kidney Int. 1984 Dec;26(6):855-60. doi: 10.1038/ki.1984.228. Kidney Int. 1984. PMID: 6533396 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

83 results

Search Page

Filters