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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 9694253)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 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. 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]  

  • 8. Family studies of the steroid 21-hydroxylase and complement C4 genes define 11 haplotypes in classical congenital adrenal hyperplasia in The Netherlands.
    Koppens PF; Hoogenboezem T; Halley DJ; Barendse CA; Oostenbrink AJ; Degenhart HJ
    Eur J Pediatr; 1992 Dec; 151(12):885-92. PubMed ID: 1473541
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel deletion alleles carrying CYP21A1P/A2 chimeric genes in Brazilian patients with 21-hydroxylase deficiency.
    Coeli FB; Soardi FC; Bernardi RD; de Araújo M; Paulino LC; Lau IF; Petroli RJ; de Lemos-Marini SH; Baptista MT; Guerra-Júnior G; de-Mello MP
    BMC Med Genet; 2010 Jun; 11():104. PubMed ID: 20587039
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Mutations in steroid 21-hydroxylase (CYP21).
    White PC; Tusie-Luna MT; New MI; Speiser PW
    Hum Mutat; 1994; 3(4):373-8. PubMed ID: 8081391
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions.
    Helmberg A; Tusie-Luna MT; Tabarelli M; Kofler R; White PC
    Mol Endocrinol; 1992 Aug; 6(8):1318-22. PubMed ID: 1406709
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency.
    Paulino LC; Araujo M; Guerra G; Marini SH; De Mello MP
    Acta Paediatr; 1999 Mar; 88(3):275-83. PubMed ID: 10229037
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease associations.
    Yang Z; Mendoza AR; Welch TR; Zipf WB; Yu CY
    J Biol Chem; 1999 Apr; 274(17):12147-56. PubMed ID: 10207042
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [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]  

  • 19. Determination of deletion sizes in the MHC-linked complement C4 and steroid 21-hydroxylase genes by pulsed-field gel electrophoresis.
    Partanen J; Kere J; Wessberg S; Koskimies S
    Genomics; 1989 Aug; 5(2):345-9. PubMed ID: 2551816
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.