BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 6607847)

  • 1. Increase of lymphocytic H-Y antigen in female 21-hydroxylase deficiency.
    Amice V; Amice J; Bercovici JP; Fauchet R
    Experientia; 1984 Mar; 40(3):273-4. PubMed ID: 6607847
    [TBL] [Abstract][Full Text] [Related]  

  • 2. H-Y positive 46 XX true hermaphroditism with intrascrotal uterus.
    Boucekkine C; Menasria A; Chouiter A; Benelkadi N; Benmiloud M
    Clin Endocrinol (Oxf); 1981 Dec; 15(6):529-35. PubMed ID: 7198944
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Increase in H-Y antigen-positive lymphocytes in hirsute women: effects of cyproterone acetate and estradiol treatment.
    Amice V; Bercovici JP; Nahoul K; Hatahet MH; Amice J
    J Clin Endocrinol Metab; 1989 Jan; 68(1):58-62. PubMed ID: 2521223
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.
    Kohn B; Levine LS; Pollack MS; Pang S; Lorenzen F; Levy D; Lerner AJ; Rondanini GF; Dupont B; New MI
    J Clin Endocrinol Metab; 1982 Nov; 55(5):817-27. PubMed ID: 6288753
    [TBL] [Abstract][Full Text] [Related]  

  • 5. H-Y antigen negative patients with testicular tissue and 46,XY karyotype.
    Haseltine FP; Genel M; Crawford JD; Breg WR
    Hum Genet; 1981; 57(3):265-8. PubMed ID: 7250968
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Research on hirsutism. Apropos of a case of partial 21-hydroxylase deficiency].
    Gheron G
    Nouv Presse Med; 1981 Oct; 10(38):3163. PubMed ID: 6974855
    [No Abstract]   [Full Text] [Related]  

  • 7. [Hirsutism secondary to congenital adrenal hyperplasia caused by a 21-hydroxylase deficiency of late onset. A clinical case].
    Zacharías S; Contreras P
    Rev Chil Obstet Ginecol; 1984; 49(5):295-9. PubMed ID: 6242254
    [No Abstract]   [Full Text] [Related]  

  • 8. Absence of H-Y antigen in XY females with dysgenetic gonads.
    Ghosh SN; Shah PN; Gharpure HM
    Nature; 1978 Nov; 276(5684):180-1. PubMed ID: 740033
    [No Abstract]   [Full Text] [Related]  

  • 9. Male pseudohermaphroditism with 17 alpha-hydroxylase deficiency.
    Scott JS
    Br J Obstet Gynaecol; 1981 Jun; 88(6):688. PubMed ID: 6972781
    [No Abstract]   [Full Text] [Related]  

  • 10. [Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups].
    Cruz-Marin F; Raffoux C; Gilgenkrantz S; Janot C; Streiff F; Pierson M
    J Genet Hum; 1981 Mar; 29(1):103-13. PubMed ID: 6977617
    [No Abstract]   [Full Text] [Related]  

  • 11. Seminoma in a 46,XX true hermaphrodite with positive H-Y antigen. A case report.
    Nichter LS
    Cancer; 1984 Mar; 53(5):1181-4. PubMed ID: 6537894
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Late onset adrenal hyperplasia (21-hydroxylase deficiency): 17-OH progesterone response to ACTH stimulation and HLA typing. A family study.
    Kauschansky A; Kaufman H; Zamir R; Elian E
    Horm Res; 1981; 14(2):73-8. PubMed ID: 6268517
    [No Abstract]   [Full Text] [Related]  

  • 13. [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]  

  • 14. [17 alpha-hydroxylase deficiency and 5 alpha-reductase deficiency].
    Yoshida H; Shimizu N
    Nihon Rinsho; 1979 Jun; 37(6):1253-9. PubMed ID: 384051
    [No Abstract]   [Full Text] [Related]  

  • 15. Studies of the C-21 and C-19 steroids and HLA genotyping in siblings and parents of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Lorenzen F; Pang S; New M; Pollack M; Oberfield S; Dupont B; Chow D; Schneider B; Levine L
    J Clin Endocrinol Metab; 1980 Mar; 50(3):572-7. PubMed ID: 6244326
    [No Abstract]   [Full Text] [Related]  

  • 16. MHC "supratype" predicting heterozygous 21-hydroxylase deficiency.
    McCluskey J; Kay PH; Stuckey M; Christiansen FT; Dawkins RL; Wilson G
    Lancet; 1983 Apr; 1(8327):764-5. PubMed ID: 6132105
    [No Abstract]   [Full Text] [Related]  

  • 17. H-Y antigen in a fertile XY female horse.
    Sharp AJ; Wachtel SS; Benirschke K
    J Reprod Fertil; 1980 Jan; 58(1):157-60. PubMed ID: 7359472
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S; Levine LS; Lorenzen F; Chow D; Pollack M; Dupont B; Genel M; New MI
    J Clin Endocrinol Metab; 1980 Mar; 50(3):586-9. PubMed ID: 6244328
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The attenuated form of congenital adrenal hyperplasia as an allelic form of 21-hydroxylase deficiency.
    Migeon CJ; Rosenwaks Z; Lee PA; Urban MD; Bias WB
    J Clin Endocrinol Metab; 1980 Sep; 51(3):647-9. PubMed ID: 6251108
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations.
    Chrousos GP; Loriaux DL; Mann D; Cutler GB
    Horm Res; 1982; 16(4):193-200. PubMed ID: 6290362
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.