141 related articles for article (PubMed ID: 2905656)
1. Prenatal DNA analysis in four embryos/fetuses at risk of 21-hydroxylase deficiency.
Matsumoto T; Kondoh T; Kamei T; Yoshimoto M; Tsuji Y; Suzumori K; Izumi R; Iwatani N; Niikawa N
Eur J Pediatr; 1988 Dec; 148(3):228-32. PubMed ID: 2905656
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency with DNA analysis.
Adachi R
Nihon Sanka Fujinka Gakkai Zasshi; 1991 Feb; 43(2):227-33. PubMed ID: 2013712
[TBL] [Abstract][Full Text] [Related]
3. Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein.
Donohoue PA; van Dop C; McLean RH; White PC; Jospe N; Migeon CJ
J Clin Endocrinol Metab; 1986 May; 62(5):995-1002. PubMed ID: 3007562
[TBL] [Abstract][Full Text] [Related]
4. HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.
White PC; New MI; Dupont B
Proc Natl Acad Sci U S A; 1984 Dec; 81(23):7505-9. PubMed ID: 6334310
[TBL] [Abstract][Full Text] [Related]
5. TaqI HLA-B and -DRB RFLP analysis can predict disease in siblings of affected children with 21-hydroxylase deficiency.
Olerup O; Luthman H; Ritzén EM; Haglund-Stengler B
Hum Genet; 1990 Oct; 85(5):467-72. PubMed ID: 1977680
[TBL] [Abstract][Full Text] [Related]
6. Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.
White PC; Grossberger D; Onufer BJ; Chaplin DD; New MI; Dupont B; Strominger JL
Proc Natl Acad Sci U S A; 1985 Feb; 82(4):1089-93. PubMed ID: 2983330
[TBL] [Abstract][Full Text] [Related]
7. Analysis of steroid 21-hydroxylase gene in five unrelated Japanese patients with 21-hydroxylase deficiency.
Nakura J; Miki T; Fukuchi K; Shimizu K; Nose O; Takai S; White PC; Honjo T; Kumahara Y
Endocrinol Jpn; 1987 Jun; 34(3):373-9. PubMed ID: 3498630
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.
Mornet E; Boue J; Raux-Demay M; Couillin P; Oury JF; Dumez Y; Dausset J; Cohen D; Boué A
Hum Genet; 1986 Aug; 73(4):358-64. PubMed ID: 3017844
[TBL] [Abstract][Full Text] [Related]
10. Diagnosis of classical steroid 21-hydroxylase deficiency using an HLA-B locus-specific DNA-probe.
Killeen AA; Seelig S; Ulstrom RA; Orr HT
Am J Med Genet; 1988 Mar; 29(3):703-12. PubMed ID: 2897792
[TBL] [Abstract][Full Text] [Related]
11. Frequent deletion and duplication of the steroid 21-hydroxylase genes.
Werkmeister JW; New MI; Dupont B; White PC
Am J Hum Genet; 1986 Oct; 39(4):461-9. PubMed ID: 3490178
[TBL] [Abstract][Full Text] [Related]
12. Gene conversions and rearrangements cause discordance between inheritance of forms of 21-hydroxylase deficiency and HLA types.
Morel Y; David M; Forest MG; Betuel H; Hauptman G; Andre J; Bertrand J; Miller WL
J Clin Endocrinol Metab; 1989 Mar; 68(3):592-9. PubMed ID: 2783935
[TBL] [Abstract][Full Text] [Related]
13. Steroid 21-hydroxylase deficiency and the major histocompatibility complex.
White PC; Werkmeister J; New MI; Dupont B
Hum Immunol; 1986 Apr; 15(4):404-15. PubMed ID: 3009365
[TBL] [Abstract][Full Text] [Related]
14. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
Pang S; Pollack MS; Loo M; Green O; Nussbaum R; Clayton G; Dupont B; New MI
J Clin Endocrinol Metab; 1985 Jul; 61(1):89-97. PubMed ID: 3873469
[TBL] [Abstract][Full Text] [Related]
15. Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency.
Mornet E; Couillin P; Kutten F; Raux MC; White PC; Cohen D; Boué A; Dausset J
Hum Genet; 1986 Dec; 74(4):402-8. PubMed ID: 2878869
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of 21-hydroxylase deficiency by the complementary deoxyribonucleic acid probe for cytochrome P-450C-21OH.
Reindollar RH; Lewis JB; White PC; Fernhoff PM; McDonough PG; Whitney JB
Am J Obstet Gynecol; 1988 Mar; 158(3 Pt 1):545-7. PubMed ID: 2831719
[TBL] [Abstract][Full Text] [Related]
17. A case of first trimester prenatal diagnosis of 21-hydroxylase deficiency with human complement C4 cDNA probe.
Nakura J; Miki T; Nishikawa K; Takemoto Y; Kamino K; Takai S; Hayashi K; Ogihara T
Endocrinol Jpn; 1990 Oct; 37(5):615-8. PubMed ID: 1982260
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. [Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency].
Couillin P
Presse Med; 1984 Apr; 13(17):1087-90. PubMed ID: 6232534
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency by steroid analysis in the amniotic fluid of mid-pregnancy: comparison with HLA typing in 17 pregnancies at risk for CAH.
Forest MG; Bétuel H; Couillin P; Boué A
Prenat Diagn; 1981 Jul; 1(3):197-207. PubMed ID: 6981108
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
