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Journal Abstract Search
220 related items for PubMed ID: 3871788
1. Ascertainment of 21-hydroxylase deficiency in individuals with HLA-B14 haplotype. Libber SM, Migeon CJ, Bias WB. J Clin Endocrinol Metab; 1985 Apr; 60(4):727-30. PubMed ID: 3871788 [Abstract] [Full Text] [Related]
5. HLA-B14 and nonclassical 21-hydroxylase deficiency in a heterogeneous New York population. Levine LS. Ann N Y Acad Sci; 1985 Apr; 458():65-70. PubMed ID: 3879132 [No Abstract] [Full Text] [Related]
6. Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families. Larizza D, Cuccia M, Martinetti M, Maghnie M, Dondi E, Salvaneschi L, Severi F. Clin Endocrinol (Oxf); 1994 Jan; 40(1):39-45. PubMed ID: 8306479 [Abstract] [Full Text] [Related]
9. An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population. Dumić M, Brkljacić L, Speiser PW, Wood E, Crawford C, Plavsić V, Baniceviác M, Radmanović S, Radica A, Kastelan A. Acta Endocrinol (Copenh); 1990 Jun; 122(6):703-10. PubMed ID: 2375234 [Abstract] [Full Text] [Related]
14. Heterozygotes and cryptic patients in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency). HLA and glyoxalase I typing and hormonal studies. Petersen KE, Svejgaard A, Nielsen MD, Dissing J. Horm Res; 1982 Jun; 16(3):151-9. PubMed ID: 6286442 [Abstract] [Full Text] [Related]