Bias WB - Search Results

1

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. Among authors: bias wb. Genomics. 1988 Jan;2(1):76-85. doi: 10.1016/0888-7543(88)90111-5. Genomics. 1988. PMID: 2838414

2

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: bias wb. J Clin Invest. 1992 Oct;90(4):1180-4. doi: 10.1172/JCI115978. J Clin Invest. 1992. PMID: 1401055 Free PMC article.

3

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: bias wb. FEBS Lett. 1990 Jan 29;260(2):183-6. doi: 10.1016/0014-5793(90)80099-5. FEBS Lett. 1990. PMID: 1688812 Free article.

4

Characterization of two hybrid C4 allotypes (C4A*12 and C4B*3) by electrophoretic, serological and restriction fragment length polymorphism analyses.

McLean RH, Bias WB, Giles C, Yu CY, Campbell RD. McLean RH, et al. Among authors: bias wb. Tissue Antigens. 1990 Feb;35(2):75-81. doi: 10.1111/j.1399-0039.1990.tb01760.x. Tissue Antigens. 1990. PMID: 1693017

5

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: bias wb. J Clin Endocrinol Metab. 1987 Nov;65(5):980-6. doi: 10.1210/jcem-65-5-980. J Clin Endocrinol Metab. 1987. PMID: 2822757

6

Neonatal lupus erythematosus syndrome: analysis of C4 allotypes and C4 genes in 18 families.

Watson RM, Scheel JN, Petri M, Lee LA, Bias WB, McLean RH. Watson RM, et al. Among authors: bias wb. Medicine (Baltimore). 1992 Mar;71(2):84-95. Medicine (Baltimore). 1992. PMID: 1545698

7

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: bias wb. 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.

8

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: bias wb. 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.

9

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: bias wb. Arthritis Rheum. 1988 Jun;31(6):736-44. doi: 10.1002/art.1780310606. Arthritis Rheum. 1988. PMID: 3260100

10

Null alleles of the fourth component of complement and HLA haplotypes in familial systemic lupus erythematosus.

Reveille JD, Arnett FC, Wilson RW, Bias WB, McLean RH. Reveille JD, et al. Among authors: bias wb. Immunogenetics. 1985;21(4):299-311. doi: 10.1007/BF00430796. Immunogenetics. 1985. PMID: 3873410

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