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 *

73 related articles for article (PubMed ID: 7603792)

  • 1. [Class I HLA antigens in children from families with congenital adrenal hyperplasia].
    Turowska-Heydel D; Pietrzyk JJ; Turowski G
    Pediatr Pol; 1995 Feb; 70(2):109-14. PubMed ID: 7603792
    [TBL] [Abstract][Full Text] [Related]  

  • 2. HLA typing of patients with 21-hydroxylase deficiency in Iranian children with congenital adrenal hyperplasia.
    Haghi Ashtiani MT; Rabbani A; Mostafavi F; Monajemzadeh M; Ranjbar Kermani F; Soltaninia J
    Biochem Genet; 2008 Dec; 46(11-12):712-9. PubMed ID: 18777204
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [HLA haplotypes in families of children with congenital adrenal hyperplasia].
    Turowska-Heydel D; Pietrzyk JJ; Turowski G
    Pediatr Pol; 1995 Feb; 70(2):115-20. PubMed ID: 7603793
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Association of HLA alleles and haplotypes with CYP21A2 gene p. V282L mutation in the Croatian population.
    Grubic Z; Maskalan M; Stingl Jankovic K; Zvecic S; Dumic Kubat K; Krnic N; Zunec R; Ille J; Kusec V; Dumic M
    HLA; 2016 Nov; 88(5):239-244. PubMed ID: 27709802
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [HLA haplotypes in congenital adrenal hyperplasia (21-hydroxylase deficiency].
    González-Díaz JP; González T; González-Espinosa C; Gantes M; Santisteban M; Bustad S
    An Esp Pediatr; 1984 Oct; 21(6):583-6. PubMed ID: 6335362
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hormonal profiles in Italian late-onset adrenal hyperplasia correlate with HLA class III polymorphisms.
    Balsamo A; Revelli A; Borelli I; Amoroso A; Cenderelli G; De Sanso G; Mazzola G; Curtoni ES; Zoppetti G; Massobrio M
    Gynecol Endocrinol; 1992 Jun; 6(2):91-8. PubMed ID: 1354409
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The HLA-A3, Cw6,B47,DR7 extended haplotypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with at least two crossover sites in the class III region.
    Donohoue PA; Guethlein L; Collins MM; Van Dop C; Migeon CJ; Bias WB; Schmeckpeper BJ
    Tissue Antigens; 1995 Sep; 46(3 ( Pt 1)):163-72. PubMed ID: 8525475
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of the association of HLA-DQ1 alleles with mutation of the 21-hydroxylase gene in patients with congenital adrenal hyperplasia].
    Osinovskaia NS; Ivashchenko TE; Baranov VS
    Genetika; 2004 Jan; 40(1):97-101. PubMed ID: 15027205
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Linkage analysis between HLA and GLOI with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Turowska-Heydel D; Sanak M; Turowska B; Pietrzyk JJ; Turowski G
    Pediatr Pol; 1995 Feb; 70(2):121-5. PubMed ID: 7603794
    [TBL] [Abstract][Full Text] [Related]  

  • 11. HLA associations in patients with polycystic ovaries and in patients with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency.
    Hague WM; Adams J; Algar V; Drummond V; Schwarz G; Bottazzo GF; Jacobs HS
    Clin Endocrinol (Oxf); 1990 Apr; 32(4):407-15. PubMed ID: 2347091
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Congenital dysfunction of adrenal cortex - detection of new mutant gene of 21-hydroxylase].
    Dzenis IG; Evgrafov OV; Brykova EK; Iudina TN; Bakharev VA; Fanchenko ND
    Vestn Ross Akad Med Nauk; 1994; (12):29-33. PubMed ID: 7742654
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Genetic considerations in light of personal studies].
    Turowska-Heydel D
    Przegl Lek; 1995; 52(1):10-2. PubMed ID: 7784603
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Clinical polymorphism of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency and HLA phenotype].
    Dzenis IG; Brykova EK; Bakharev VA
    Akush Ginekol (Mosk); 1990 Jan; (1):10-4. PubMed ID: 2353725
    [No Abstract]   [Full Text] [Related]  

  • 15. Coupling of HLA-A3,Cw6,Bw47,DR7 and a normal CA21HB steroid 21-hydroxylase gene in the Old Order Amish.
    Donohoue PA; Van Dop C; Migeon CJ; McLean RH; Bias WB
    J Clin Endocrinol Metab; 1987 Nov; 65(5):980-6. PubMed ID: 2822757
    [TBL] [Abstract][Full Text] [Related]  

  • 16. HLA haplotypes and hormonal studies in 25 Italian families of patients with classical and non-classical 21-OH deficiency.
    Einaudi S; Borelli I; Lala R; Praticŏ L; Curtoni ES; De Sanctis C
    J Pediatr Endocrinol; 1994; 7(4):349-55. PubMed ID: 7735374
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Layrisse Z; White C; Gunczler P; Gafaro Valera L; Arias S; Yunis EJ; Alper CA; Awdeh ZL
    Immunogenetics; 1987; 25(2):99-103. PubMed ID: 3493216
    [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. Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.
    Levine LS; Dupont B; Lorenzen F; Pang S; Pollack M; Oberfield S; Kohn B; Lerner A; Cacciari E; Mantero F; Cassio A; Scaroni C; Chiumello G; Rondanini GF; Gargantini L; Giovannelli G; Virdis R; Bartolotta E; Migliori C; Pintor C; Tato L; Barboni F; New MI
    J Clin Endocrinol Metab; 1980 Dec; 51(6):1316-24. PubMed ID: 6449518
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Distribution of the V281L mutation of the CYP21 gene in Israeli congenital adrenal hyperplasia patients and its association with HLA- B14.
    Israel S; Weinrib L; Weintrob N; Miller K; Brautbar C
    Pediatr Endocrinol Rev; 2006 Aug; 3 Suppl 3():447-50. PubMed ID: 17551464
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.