BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 2613228)

  • 1. Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21B.
    Donohoue PA; Jospe N; Migeon CJ; Van Dop C
    Genomics; 1989 Oct; 5(3):397-406. PubMed ID: 2613228
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes.
    Collier S; Sinnott PJ; Dyer PA; Price DA; Harris R; Strachan T
    EMBO J; 1989 May; 8(5):1393-402. PubMed ID: 2788573
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exon 7 Ncol restriction site within CYP21B (steroid 21-hydroxylase) is a normal polymorphism.
    Donohoue PA; Sandrini Neto R; Collins MM; Migeon CJ
    Mol Endocrinol; 1990 Sep; 4(9):1354-62. PubMed ID: 1978247
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Major-histocompatibility-complex gene markers and restriction-fragment analysis of steroid 21-hydroxylase (CYP21) and complement C4 genes in classical congenital adrenal hyperplasia patients in a single population.
    Partanen J; Koskimies S; Sipilä I; Lipsanen V
    Am J Hum Genet; 1989 May; 44(5):660-70. PubMed ID: 2565078
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Mutations in 21-hydroxylase gene caused by gene conversion-like events].
    Urabe K
    Fukuoka Igaku Zasshi; 1990 Feb; 81(2):77-87. PubMed ID: 2328938
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.
    White PC; Vitek A; Dupont B; New MI
    Proc Natl Acad Sci U S A; 1988 Jun; 85(12):4436-40. PubMed ID: 3260033
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia.
    Ghanem N; Lobaccaro JM; Buresi C; Abbal M; Halaby G; Sultan C; Lefranc G
    Hum Genet; 1990 Dec; 86(2):117-25. PubMed ID: 1979956
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.
    Sinnott P; Collier S; Costigan C; Dyer PA; Harris R; Strachan T
    Proc Natl Acad Sci U S A; 1990 Mar; 87(6):2107-11. PubMed ID: 2315306
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.
    Amor M; Parker KL; Globerman H; New MI; White PC
    Proc Natl Acad Sci U S A; 1988 Mar; 85(5):1600-4. PubMed ID: 3257825
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gene conversion in steroid 21-hydroxylase genes.
    Urabe K; Kimura A; Harada F; Iwanaga T; Sasazuki T
    Am J Hum Genet; 1990 Jun; 46(6):1178-86. PubMed ID: 1971153
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CYP21B gene conversion and complete CYP21A gene deletion in congenital adrenal hyperplasia.
    Lobaccaro JM; Ghanem N; Lefranc G; Sultan C
    Ann Genet; 1990; 33(2):70-5. PubMed ID: 1978631
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Direct analysis of CYP21B genes in 21-hydroxylase deficiency using polymerase chain reaction amplification.
    Owerbach D; Crawford YM; Draznin MB
    Mol Endocrinol; 1990 Jan; 4(1):125-31. PubMed ID: 2325662
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of the recombination site within the steroid 21-hydroxylase gene (CYP21) of the HLA-B47,DR7 haplotype.
    Chu X; Braun-Heimer L; Rittner C; Schneider PM
    Exp Clin Immunogenet; 1992; 9(2):80-5. PubMed ID: 1489553
    [TBL] [Abstract][Full Text] [Related]  

  • 14. High variability of CYP21 gene rearrangements in Spanish patients with classic form of congenital adrenal hyperplasia.
    Lobato MN; Aledo R; Meseguer A
    Hum Hered; 1998; 48(4):216-25. PubMed ID: 9694253
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families.
    Sinnott PJ; Livieri C; Sampietro M; Marconi M; Harris R; Severi F; Strachan T
    Hum Genet; 1992 Mar; 88(5):545-51. PubMed ID: 1551657
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency.
    Rumsby G; Fielder AH; Hague WM; Honour JW
    J Med Genet; 1988 Sep; 25(9):596-9. PubMed ID: 3263505
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency.
    Mornet E; Crété P; Kuttenn F; Raux-Demay MC; Boué J; White PC; Boué A
    Am J Hum Genet; 1991 Jan; 48(1):79-88. PubMed ID: 1985465
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of molecular defects causing congenital adrenal hyperplasia by cloning and differential hybridization of polymerase chain reaction-amplified 21-hydroxylase (CYP21) genes.
    Helmberg A; Tabarelli M; Fuchs MA; Keller E; Dobler G; Schnegg I; Knorr D; Albert E; Kofler R
    DNA Cell Biol; 1992 Jun; 11(5):359-68. PubMed ID: 1605859
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Altered CYP21 genes in HLA-haplotypes associated with congenital adrenal hyperplasia (CAH): a family study.
    Manfras BJ; Swinyard M; Rudert WA; Ball EJ; Lee PA; Kühnl P; Trucco M; Böhm BO
    Hum Genet; 1993 Aug; 92(1):33-9. PubMed ID: 8365724
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pseudogene/functional gene ratio in late-onset 21-hydroxylase-deficient adrenal hyperplasia.
    Azziz R; Wells G; Acton RT; Zacur HA
    Am J Obstet Gynecol; 1990 Mar; 162(3):633-8. PubMed ID: 2316563
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.