102 related articles for article (PubMed ID: 1982260)
1. 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]
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. 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]
5. RFLPs of 21-hydroxylase and C4 genes: application to pedigree analysis on 21-hydroxylase deficiency.
Matsumoto T; Kondoh T; Baba T; Yoshimoto M; Niikawa N; Tsuji Y
Acta Paediatr Jpn; 1988; 30 Suppl():111-6. PubMed ID: 2906201
[No Abstract] [Full Text] [Related]
6. 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]
7. Prenatal diagnosis of 21-hydroxylase deficiency by RFLP analysis of the 21-hydroxylase, complement C4, and HLA class II genes.
Keller E; Andreas A; Scholz S; Dörr HC; Knorr D; Albert ED
Prenat Diagn; 1991 Nov; 11(11):827-40. PubMed ID: 1684434
[TBL] [Abstract][Full Text] [Related]
8. First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency).
Speiser PW; Laforgia N; Kato K; Pareira J; Khan R; Yang SY; Whorwood C; White PC; Elias S; Schriock E
J Clin Endocrinol Metab; 1990 Apr; 70(4):838-48. PubMed ID: 1969421
[TBL] [Abstract][Full Text] [Related]
9. A rare TaqI polymorphism in a human complement C4 gene is caused by an additional restriction site in the first intron.
Koppens PF; Hoogenboezem T; Degenhart HJ
Immunol Lett; 1992; 34(2):93-7. PubMed ID: 1362564
[TBL] [Abstract][Full Text] [Related]
10. HLA class I-, complement C4- and 21-hydroxylase probes in the genetic analysis of 21-hydroxylase deficiency.
Kochhan L; Janssen S; Knorr D; Olek K; Bidlingmaier F
J Clin Chem Clin Biochem; 1990 Jun; 28(6):413-7. PubMed ID: 2212957
[TBL] [Abstract][Full Text] [Related]
11. Associations between restriction fragment length polymorphisms detected with a probe for human C4 and allotype of C4B5 allele.
Kobayashi K; Atoh M; Hara M; Tanaka H; Itoh K; Hirakawa K; Sekiguchi S
Hum Immunol; 1990 Sep; 29(1):3-13. PubMed ID: 1976612
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of infantile hypophosphatasia.
Kishi F; Matsuura S; Murano I; Akita A; Kajii T
Prenat Diagn; 1991 May; 11(5):305-9. PubMed ID: 1680232
[TBL] [Abstract][Full Text] [Related]
13. Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiency.
Haglund-Stengler B; Martin Ritzén E; Gustafsson J; Luthman H
Proc Natl Acad Sci U S A; 1991 Oct; 88(19):8352-6. PubMed ID: 1924294
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blot.
Speiser PW; White PC; Dupont J; Zhu D; Mercado AB; New MI
Hum Genet; 1994 Apr; 93(4):424-8. PubMed ID: 8168813
[TBL] [Abstract][Full Text] [Related]
16. [Prenatal molecular genetic diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
Rodríguez A; Ezquieta B; Varela JM; Moreno M; Dulín E; Rodríguez Arnao MD
Med Clin (Barc); 1997 Nov; 109(17):669-72. PubMed ID: 9488957
[TBL] [Abstract][Full Text] [Related]
17. A rare complement component C4 restriction fragment length polymorphism in two families with systemic lupus erythematosus.
Goldstein R; Moulds JM; Sengar DP
J Rheumatol; 1991 Mar; 18(3):345-8. PubMed ID: 1677422
[TBL] [Abstract][Full Text] [Related]
18. Successful prenatal treatment of congenital adrenal hyperplasia resulting from the 21-hydroxylase deficiency: is prenatal diagnosis in a mother at risk essential?
Romer TE; Ginalska-Malinowska M
Endokrynol Pol; 1987; 38(1):125-30. PubMed ID: 3428229
[No Abstract] [Full Text] [Related]
19. Restriction fragment length polymorphism study of families with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Taiwan.
Lee JS; Tsai HM; Shieh RP; Chen SH; Tsai WY; Chung BC
J Formos Med Assoc; 1990 Jul; 89(7):534-40. PubMed ID: 1979594
[TBL] [Abstract][Full Text] [Related]
20. Definitive RFLPs to distinguish between the human complement C4A/C4B isotypes and the major Rodgers/Chido determinants: application to the study of C4 null alleles.
Yu CY; Campbell RD
Immunogenetics; 1987; 25(6):383-90. PubMed ID: 2439447
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
