These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
153 related articles for article (PubMed ID: 2613228)
61. Molecular analysis of CYP21 and C4 genes in Brazilian families with the classical form of steroid 21-hydroxylase deficiency. de-Araujo M; Sanches MR; Suzuki LA; Guerra G; Farah SB; de-Mello MP Braz J Med Biol Res; 1996 Jan; 29(1):1-13. PubMed ID: 8731325 [TBL] [Abstract][Full Text] [Related]
62. Nonisotopic identification of two point mutations in the CYP21 gene responsible for nonclassic 21-hydroxylase deficiency. Shevtsov SP; Rechitsky S; Verlinsky O; Schwartz EI Biochem Med Metab Biol; 1994 Aug; 52(2):85-8. PubMed ID: 7993665 [TBL] [Abstract][Full Text] [Related]
63. CYP21 pseudogene transcripts are much less abundant than those from the active gene in normal human adrenocortical cells under various conditions in culture. Endoh A; Yang L; Hornsby PJ Mol Cell Endocrinol; 1998 Feb; 137(1):13-9. PubMed ID: 9607724 [TBL] [Abstract][Full Text] [Related]
64. Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia. Lee HH; Chao HT; Ng HT; Choo KB J Med Genet; 1996 May; 33(5):371-5. PubMed ID: 8733045 [TBL] [Abstract][Full Text] [Related]
65. A method for specific amplification and PCR sequencing of individual members of multigene families: application to the study of steroid 21-hydroxylase deficiency. Collier S; Tassabehji M; Strachan T PCR Methods Appl; 1992 Feb; 1(3):181-6. PubMed ID: 1472941 [TBL] [Abstract][Full Text] [Related]
66. Simultaneous detection of five mutations in the steroid 21-hydroxylase gene using nested allele-specific amplification. Rothberg PG; Baker DW; Bradley JF Genet Test; 1998; 2(4):343-6. PubMed ID: 10464614 [TBL] [Abstract][Full Text] [Related]
67. Molecular analysis of patient and carrier genes with congenital steroid 21-hydroxylase deficiency by using polymerase chain reaction and single strand conformation polymorphism. Tajima T; Fujieda K; Nakayama K; Fujii-Kuriyama Y J Clin Invest; 1993 Nov; 92(5):2182-90. PubMed ID: 8227333 [TBL] [Abstract][Full Text] [Related]
68. Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia. Harada F; Kimura A; Iwanaga T; Shimozawa K; Yata J; Sasazuki T Proc Natl Acad Sci U S A; 1987 Nov; 84(22):8091-4. PubMed ID: 3500473 [TBL] [Abstract][Full Text] [Related]
69. [A molecular method of diagnosis of congenital adrenal hyperplasia]. Israel S; Brautbar C Harefuah; 2000 Dec; 139(11-12):429-33, 494. PubMed ID: 11341187 [TBL] [Abstract][Full Text] [Related]
70. E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Kirby-Keyser L; Porter CC; Donohoue PA Hum Mutat; 1997; 9(2):181-2. PubMed ID: 9067760 [No Abstract] [Full Text] [Related]
72. DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia. Partanen J; Koskimies S; Sipilä I Hum Genet; 1988 Apr; 78(4):372-3. PubMed ID: 2896160 [TBL] [Abstract][Full Text] [Related]