124 related articles for article (PubMed ID: 6266985)
1. Intra-HLA recombinations localizing the 21-hydroxylase deficiency gene within the HLA complex.
Bias WB; Urban MD; Migeon CJ; Hsu SH; Lee PA
Hum Immunol; 1981 Mar; 2(2):139-45. PubMed ID: 6266985
[TBL] [Abstract][Full Text] [Related]
2. HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency.
Stuckey MS; Boyne P; Macdonald WB; Christiansen FT; Houliston JB; Dawkins RL
Aust N Z J Med; 1980 Oct; 10(5):552-4. PubMed ID: 6258552
[TBL] [Abstract][Full Text] [Related]
3. 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; 16(3):151-9. PubMed ID: 6286442
[TBL] [Abstract][Full Text] [Related]
4. Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Layrisse Z; White C; Gunczler P; Gafaro Valera L; Arias S; Yunis EJ; Alper CA; Awdeh ZL
Immunogenetics; 1987; 25(2):99-103. PubMed ID: 3493216
[TBL] [Abstract][Full Text] [Related]
5. Complotype genetic loci segregate more frequently with HLA-DR than with HLA-B.
Yunis EJ; Awdeh Z; Johnson A; Suciu-Foca N; Robinson MA; Hartzman R; Raum D; Fleischnick E; Alper CA
Immunogenetics; 1985; 21(1):25-31. PubMed ID: 3871424
[TBL] [Abstract][Full Text] [Related]
6. Late-onset form of congenital adrenal hyperplasia in the HLA-B14; DR1 haplotype is caused by a duplication in the 21-OH MHC gene region.
Boehm BO; Rosak C; Kuehnl P; Schöffling K
Horm Metab Res; 1986 Nov; 18(11):791-2. PubMed ID: 3491779
[No Abstract] [Full Text] [Related]
7. Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1.
Speiser PW; New MI; White PC
N Engl J Med; 1988 Jul; 319(1):19-23. PubMed ID: 3260007
[TBL] [Abstract][Full Text] [Related]
8. 21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patients.
Livieri C; Belvedere M; Martinetti M; Beluffi G; Fiori P; Cogliati CR; Goffredo V; Lorini R; Severi F
Prog Clin Biol Res; 1985; 200():243-55. PubMed ID: 3001775
[No Abstract] [Full Text] [Related]
9. Anomalous mixed lymphocyte culture reactivity between HLA--A, --B, --C, --DR identical siblings.
Reinsmoen NL; Noreen HJ; Friend PS; Giblett ER; Greenberg LJ; Kersey JH
Tissue Antigens; 1979 Jan; 13(1):19-34. PubMed ID: 154195
[TBL] [Abstract][Full Text] [Related]
10. The attenuated form of congenital adrenal hyperplasia as an allelic form of 21-hydroxylase deficiency.
Migeon CJ; Rosenwaks Z; Lee PA; Urban MD; Bias WB
J Clin Endocrinol Metab; 1980 Sep; 51(3):647-9. PubMed ID: 6251108
[TBL] [Abstract][Full Text] [Related]
11. [Genetic of the 21 hydroxylase deficiency].
Boué A; Couillin P; Pomarède R; Rappaport R; Boué J
Ann Endocrinol (Paris); 1982; 43(1):3-14. PubMed ID: 6982657
[TBL] [Abstract][Full Text] [Related]
12. Defective antigen presentation and novel structural properties of DR1 from an HLA haplotype associated with 21-hydroxylase deficiency.
Davis JE; Rich RR; Van M; Le HV; Pollack MS; Cook RG
J Clin Invest; 1987 Oct; 80(4):998-1008. PubMed ID: 2443540
[TBL] [Abstract][Full Text] [Related]
13. Basic and clinical aspects of congenital adrenal hyperplasia.
New MI
J Steroid Biochem; 1987; 27(1-3):1-7. PubMed ID: 3320531
[TBL] [Abstract][Full Text] [Related]
14. The HLA associations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a Yugoslav population.
Kastelan A; Brkljacić-Surkalović L; Dumić M
Ann N Y Acad Sci; 1985; 458():36-40. PubMed ID: 3879128
[No Abstract] [Full Text] [Related]
15. Genetics and biochemical variability of variants of 21 hydroxylase deficiency.
Gordon MT; Conway DI; Anderson DC; Harris R
J Med Genet; 1985 Oct; 22(5):354-60. PubMed ID: 3001309
[TBL] [Abstract][Full Text] [Related]
16. The coexistence of IgA deficiency and 21-hydroxylase deficiency marked by specific MHC supratypes.
Cobain TJ; Stuckey MS; McCluskey J; Wilton AN; Gedeon A; Garlepp MJ; Christiansen FT; Dawkins RL
Ann N Y Acad Sci; 1985; 458():76-84. PubMed ID: 3879134
[No Abstract] [Full Text] [Related]
17. MHC "supratype" predicting heterozygous 21-hydroxylase deficiency.
McCluskey J; Kay PH; Stuckey M; Christiansen FT; Dawkins RL; Wilson G
Lancet; 1983 Apr; 1(8327):764-5. PubMed ID: 6132105
[No Abstract] [Full Text] [Related]
18. [HLA antigens and different clinical forms of 21-hydroxylase deficiency in the French population].
Couillin P; Ravisé N; Hors J; Feingold J; Rappaport R; Kuttenn F; Boué A
Pathol Biol (Paris); 1986 Jun; 34(6):789-94. PubMed ID: 3531997
[TBL] [Abstract][Full Text] [Related]
19. Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.
Laron Z; Pollack MS; Zamir R; Roitman A; Dickerman Z; Levine LS; Lorenzen F; O'Neill GJ; Pang S; New MI; Dupont B
Hum Immunol; 1980 Jul; 1(1):55-66. PubMed ID: 6266983
[No Abstract] [Full Text] [Related]
20. Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Lee PA; Rosenwaks Z; Urban MD; Migeon CJ; Bias WD
J Clin Endocrinol Metab; 1982 Nov; 55(5):866-71. PubMed ID: 6288754
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]