White PC - Search Results

1

Molecular genetics of congenital adrenal hyperplasia.

White PC, New MI. White PC, et al. Baillieres Clin Endocrinol Metab. 1988 Nov;2(4):941-65. doi: 10.1016/s0950-351x(88)80025-9. Baillieres Clin Endocrinol Metab. 1988. PMID: 3077248 Review.

2

Genetic basis of endocrine disease 2: congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

White PC, New MI. White PC, et al. J Clin Endocrinol Metab. 1992 Jan;74(1):6-11. doi: 10.1210/jcem.74.1.1727830. J Clin Endocrinol Metab. 1992. PMID: 1727830 Review. No abstract available.

3

Fertility in patients with congenital adrenal hyperplasia.

Reichman DE, White PC, New MI, Rosenwaks Z. Reichman DE, et al. Among authors: white pc. Fertil Steril. 2014 Feb;101(2):301-9. doi: 10.1016/j.fertnstert.2013.11.002. Epub 2013 Dec 17. Fertil Steril. 2014. PMID: 24355046 Free article. Review.

4

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.

White PC, Grossberger D, Onufer BJ, Chaplin DD, New MI, Dupont B, Strominger JL. White PC, et al. Proc Natl Acad Sci U S A. 1985 Feb;82(4):1089-93. doi: 10.1073/pnas.82.4.1089. Proc Natl Acad Sci U S A. 1985. PMID: 2983330 Free PMC article.

5

Steroid 21-hydroxylase deficiency and the major histocompatibility complex.

White PC, Werkmeister J, New MI, Dupont B. White PC, et al. Hum Immunol. 1986 Apr;15(4):404-15. doi: 10.1016/0198-8859(86)90018-2. Hum Immunol. 1986. PMID: 3009365

6

Immunohistochemistry of cytochrome P-450 21-hydroxylase: microscopic examination of the enzyme in the bovine adrenal cortex and kidney.

Sasano H, White PC, New MI, Sasano N. Sasano H, et al. Among authors: white pc. Endocrinology. 1988 Jan;122(1):291-5. doi: 10.1210/endo-122-1-291. Endocrinology. 1988. PMID: 3257188

7

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.

Amor M, Parker KL, Globerman H, New MI, White PC. Amor M, et al. Among authors: white pc. Proc Natl Acad Sci U S A. 1988 Mar;85(5):1600-4. doi: 10.1073/pnas.85.5.1600. Proc Natl Acad Sci U S A. 1988. PMID: 3257825 Free PMC article.

8

Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1.

Speiser PW, New MI, White PC. Speiser PW, et al. Among authors: white pc. N Engl J Med. 1988 Jul 7;319(1):19-23. doi: 10.1056/NEJM198807073190104. N Engl J Med. 1988. PMID: 3260007

9

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.

White PC, Vitek A, Dupont B, New MI. White PC, et al. Proc Natl Acad Sci U S A. 1988 Jun;85(12):4436-40. doi: 10.1073/pnas.85.12.4436. Proc Natl Acad Sci U S A. 1988. PMID: 3260033 Free PMC article.

10

Nonsense mutation causing steroid 21-hydroxylase deficiency.

Globerman H, Amor M, Parker KL, New MI, White PC. Globerman H, et al. Among authors: white pc. J Clin Invest. 1988 Jul;82(1):139-44. doi: 10.1172/JCI113562. J Clin Invest. 1988. PMID: 3267225 Free PMC article.

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