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24. [Genetics of congenital adrenal hyperplasia caused by steroid-21-hydroxylase deficiency: present-day aspects]. Moreno Aznar L; Sarriá Chueca A; Bueno Lozano G; Bueno Sánchez M An Esp Pediatr; 1988 Jun; 28(6):531-6. PubMed ID: 3057971 [TBL] [Abstract][Full Text] [Related]
25. [21-hydroxylase deficiency: a case in a newborn revealing a maternal forme tardive]. Simonin G; Palix C; Roulier R; Coignet J Ann Pediatr (Paris); 1986 May; 33(5):423-7. PubMed ID: 3729253 [No Abstract] [Full Text] [Related]
26. Congenital adrenal hyperplasia. New MI; Levine LS Monogr Endocrinol; 1984; 26():1-88. PubMed ID: 6472279 [TBL] [Abstract][Full Text] [Related]
27. [The eugenic significance of HLA determination in congenital adrenal hyperplasia]. Li XQ Zhonghua Yi Xue Za Zhi; 1984 Feb; 64(2):105-7. PubMed ID: 6432246 [No Abstract] [Full Text] [Related]
28. [Molecular biology of the adrenogenital syndrome. New possibilities of heterozygote screening]. Böhm BO; Rosak C; Böhm TL; White PC; Schöffling K Dtsch Med Wochenschr; 1987 Jan; 112(3):87-9. PubMed ID: 3492354 [TBL] [Abstract][Full Text] [Related]
29. [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]
31. HLA typing as a method of genetic counselling in congenital adrenal hyperplasia. Savage MO; Field H; Wolf E; Pembrey ME; Grant DB Arch Dis Child; 1982 Apr; 57(4):315-7. PubMed ID: 6979315 [TBL] [Abstract][Full Text] [Related]
32. HLA and congenital adrenal hyperplasia due to 11-hydroxylase deficiency. Glenthøj A; Nielsen MD; Starup J; Svejgaard A Tissue Antigens; 1979 Aug; 14(2):181-2. PubMed ID: 494231 [No Abstract] [Full Text] [Related]
33. Detection of heterozygote of 21-hydroxylase deficiency. Sobel DO; Gutai JP; Jones JC; Wagener DK; Smith W Lancet; 1980 Jan; 1(8158):47. PubMed ID: 6101388 [No Abstract] [Full Text] [Related]
34. Genetics of acquired and congenital adrenal hyperplasia. Morillo E; Gardner LI Lancet; 1979 Jul; 2(8135):202-3. PubMed ID: 89316 [No Abstract] [Full Text] [Related]
35. Linkage and segregation analysis of HLA and congenital hypoaldosteronism due to corticosterone methyl-oxydase deficiency type I and type II. de Jongh BM; Veldhuis JD; Drop SL; Nijenhuis LE; Dupont B Tissue Antigens; 1984 Jul; 24(1):18-24. PubMed ID: 6592791 [TBL] [Abstract][Full Text] [Related]
37. [Linkage between the gene responsible for adrenal hyperplasia caused by 21-hydroxylase deficiency and chromosome-6 short-arm markers]. Flori J; Tongio MM; Kurtz F; Mayer S; Juif JG J Genet Hum; 1981 Feb; 28(5):185-93. PubMed ID: 6974227 [TBL] [Abstract][Full Text] [Related]
38. [Genetics of the HLA system and major histocompatibility complex]. Lambotte C Rev Med Liege; 1983 Feb; 38(4):118-27. PubMed ID: 6844774 [No Abstract] [Full Text] [Related]
39. Compensatory growth after HLA-typing revelation of incorrect diagnosis of 21-hydroxylase deficiency. Sobel EH; Hahm SY Acta Endocrinol Suppl (Copenh); 1986; 279():290-4. PubMed ID: 3465170 [TBL] [Abstract][Full Text] [Related]