van Dop C - 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: van dop c. 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: van dop c. 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

Congenital adrenal hyperplasia: molecular mechanisms resulting in 21-hydroxylase deficiency.

Donohoue PA, Van Dop C, Jospe N, Migeon CJ. Donohoue PA, et al. Among authors: van dop c. Acta Endocrinol Suppl (Copenh). 1986;279:315-20. doi: 10.1530/acta.0.112s315. Acta Endocrinol Suppl (Copenh). 1986. PMID: 3022524 Review.

4

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: van dop c. 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.

5

Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21B.

Donohoue PA, Jospe N, Migeon CJ, Van Dop C. Donohoue PA, et al. Among authors: van dop c. Genomics. 1989 Oct;5(3):397-406. doi: 10.1016/0888-7543(89)90002-5. Genomics. 1989. PMID: 2613228

6

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: van dop c. Genomics. 1988 Jan;2(1):76-85. doi: 10.1016/0888-7543(88)90111-5. Genomics. 1988. PMID: 2838414

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: van dop c. 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

The HLA-A3, Cw6,B47,DR7 extended haplotypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with at least two crossover sites in the class III region.

Donohoue PA, Guethlein L, Collins MM, Van Dop C, Migeon CJ, Bias WB, Schmeckpeper BJ. Donohoue PA, et al. Among authors: van dop c. Tissue Antigens. 1995 Sep;46(3 ( Pt 1)):163-72. doi: 10.1111/j.1399-0039.1995.tb03115.x. Tissue Antigens. 1995. PMID: 8525475

9

McCune-Albright syndrome. Long-term follow-up.

Lee PA, Van Dop C, Migeon CJ. Lee PA, et al. Among authors: van dop c. JAMA. 1986 Dec 5;256(21):2980-4. JAMA. 1986. PMID: 3773215

10

Enhanced growth with growth hormone therapy after renal transplantation.

Van Dop C, Donohoue PA, Bock GH, Ruley J. Van Dop C, et al. Pediatr Nephrol. 1989 Oct;3(4):468-9. doi: 10.1007/BF00850231. Pediatr Nephrol. 1989. PMID: 2642119 No abstract available.

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