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The Journal of Steroid Biochemistry and Molecular Biology|March 1, 1992
Prenatal diagnosis/treatment in families at risk for infants with steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia)L P Karaviti, A B Mercado, M B Mercado, et al.
The New England Journal of Medicine|October 26, 1978
Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage groupL S Levine, M Zachmann, M I New, et al.
Journal of Hepatology|January 1, 1986
Resolution of the clinical features of tyrosinemia following orthotopic liver transplantation for hepatomaD H Van Thiel, L M Gartner, F K Thorp, et al.
Hormones and Behavior|December 1, 1996
Gender change from female to male in classical congenital adrenal hyperplasiaH F Meyer-Bahlburg, R S Gruen, M I New, et al.
Pediatric Research|December 1, 1984
Biochemical studies of a patient with hereditary hepatorenal tyrosinemia: evidence of glutathione deficiencyE Stoner, H Starkman, D Wellner, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1982
Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasiaB Kohn, L S Levine, M S Pollack, et al.
American Journal of Human Genetics|July 1, 1981
HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiencyM S Pollack, L S Levine, G J O'Neill, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1976
Presence of H-Y antigen and testis in 46, XX true hermaphroditism, evidence for Y-chromosomal functionP Saenger, L S Levine, S S Wachtel, et al.
The Journal of Clinical Endocrinology and Metabolism|December 12, 2001
Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnanciesM I New, A Carlson, J Obeid, et al.
The Journal of Bone and Joint Surgery. American Volume|January 1, 1988
Induction and characterization of an interface tissue by implantation of methylmethacrylate cement into the posterior part of the cervical spine of the dogR Whitehill, S Drucker, J A McCoig, et al.
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