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 *

75 related articles for article (PubMed ID: 7603793)

  • 1. [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]  

  • 2. [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]  

  • 3. 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]  

  • 4. [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]  

  • 5. [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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Late-onset form of congenital adrenal hyperplasia in the HLA-B14; DR1 haplotype is caused by a duplication in the 21-OH MHC gene region.
    Boehm BO; Rosak C; Kuehnl P; Schöffling K
    Horm Metab Res; 1986 Nov; 18(11):791-2. PubMed ID: 3491779
    [No Abstract]   [Full Text] [Related]  

  • 11. [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]  

  • 12. Preliminary investigation of mutations in 21-hydroxylase gene in patients with congenital adrenal hyperplasia in Russia.
    Evgrafov OV; Polyakov AV; Dzenis IG; Baharev VA
    Hum Mutat; 1995; 5(2):131-6. PubMed ID: 7749411
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients.
    Fleischnick E; Awdeh ZL; Raum D; Granados J; Alosco SM; Crigler JF; Gerald PS; Giles CM; Yunis EJ; Alper CA
    Lancet; 1983 Jan; 1(8317):152-6. PubMed ID: 6130199
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Study of Human Leukocyte Antigen (HLA) in 13 cases of familial frontal fibrosing alopecia: CYP21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA-A*33:01; B*14:02; C*08:02 as a genetic marker.
    Porriño-Bustamante ML; López-Nevot MÁ; Aneiros-Fernández J; Casado-Ruiz J; García-Linares S; Pedrinacci-Rodríguez S; García-Lora E; Martín-Casares MA; Fernández-Pugnaire MA; Arias-Santiago S
    Australas J Dermatol; 2019 Aug; 60(3):e195-e200. PubMed ID: 30656636
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [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]  

  • 17. [Steroid 21-hydroxylase deficiency--congenital adrenal hyperplasia].
    Urabe K; Harada F; Sasazuki T
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):903-8. PubMed ID: 3270907
    [No Abstract]   [Full Text] [Related]  

  • 18. HLA haplotypes in children with adrenogenital syndrome and their parents.
    László A; Godó B; Kaiser G; Hajdu J; Fazekas C
    Acta Paediatr Acad Sci Hung; 1981; 22(3):217-22. PubMed ID: 7304161
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Late-onset type of 21-hydroxylase deficiency in childhood.
    Roitman A; Stivel M; Zamir R; Kaufman H; Pertzelan A; Laron Z
    Isr J Med Sci; 1982 Jul; 18(7):763-8. PubMed ID: 6980865
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The infantile form of sialidosis type II associated with congenital adrenal hyperplasia: possible linkage between HLA and the neuraminidase deficiency gene.
    Oohira T; Nagata N; Akaboshi I; Matsuda I; Naito S
    Hum Genet; 1985; 70(4):341-3. PubMed ID: 3874816
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.