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Journal Abstract Search

175 related items for PubMed ID: 6130199

  • 1. 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 22; 1(8317):152-6. PubMed ID: 6130199
    [Abstract] [Full Text] [Related]

  • 2. Human MHC class III (Bf, C2, C4) genes and GLO: their association with other HLA antigens and extended haplotypes in the Spanish population.
    Regueiro JR, Arnaiz-Villena A.
    Tissue Antigens; 1988 Jan 22; 31(1):14-25. PubMed ID: 3341017
    [Abstract] [Full Text] [Related]

  • 3. 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 Jan 22; 25(2):99-103. PubMed ID: 3493216
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  • 5. 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 22; 65(5):980-6. PubMed ID: 2822757
    [Abstract] [Full Text] [Related]

  • 6. HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency.
    Pollack MS, New MI, O'Neill GJ, Levine LS, Callaway C, Pang S, 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, Dupont B.
    Hum Genet; 1981 Nov 22; 58(3):331-7. PubMed ID: 6948766
    [Abstract] [Full Text] [Related]

  • 7. Class III alleles and high-risk MHC haplotypes in type I diabetes mellitus, Graves' disease and Hashimoto's thyroiditis.
    Skanes VM, Barnard J, Farid N, Marshall WH, Murphy L, Rideout D, Taylor R, Xidos G, Larsen B.
    Mol Biol Med; 1986 Apr 22; 3(2):143-57. PubMed ID: 3461234
    [Abstract] [Full Text] [Related]

  • 8. The HLA system in the Korean population.
    Kim SJ, Nisperos B, Mickelson E, Choi IH, Dahlberg S, Kim JD, Giblett ER, Hansen JA.
    Hum Immunol; 1986 Nov 22; 17(3):259-72. PubMed ID: 3793531
    [Abstract] [Full Text] [Related]

  • 9. 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 22; 92(1):33-9. PubMed ID: 8365724
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  • 11. Italian extended HLA haplotypes in congenital adrenal hyperplasia.
    Abbal M, Belvedere MC, Livieri C, De Paoli F, Martinetti M, Severi F, Cambon-Thomsen A.
    Tissue Antigens; 1988 Jul 22; 32(1):17-23. PubMed ID: 3263715
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  • 13. Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathy.
    Alper CA, Fleischnick E, Awdeh Z, Katz AJ, Yunis EJ.
    J Clin Invest; 1987 Jan 22; 79(1):251-6. PubMed ID: 3793924
    [Abstract] [Full Text] [Related]

  • 14. Steroid 21-hydroxylase deficiency and the major histocompatibility complex.
    White PC, Werkmeister J, New MI, Dupont B.
    Hum Immunol; 1986 Apr 22; 15(4):404-15. PubMed ID: 3009365
    [Abstract] [Full Text] [Related]

  • 15. Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man.
    Awdeh ZL, Raum D, Yunis EJ, Alper CA.
    Proc Natl Acad Sci U S A; 1983 Jan 22; 80(1):259-63. PubMed ID: 6401863
    [Abstract] [Full Text] [Related]

  • 16. Gene frequencies and genetic linkage disequilibrium for the HLA-linked genes Bf, C2, C4S, C4F, 21-hydroxylase deficiency, and glyoxalase I.
    O'Neill GJ, Pollack MS, Yang SY, Levine LS, New MI, Dupont B.
    Transplant Proc; 1979 Dec 22; 11(4):1713-5. PubMed ID: 316936
    [No Abstract] [Full Text] [Related]

  • 17. Complement genes of the major histocompatibility complex (complotypes), extended haplotypes and disease markers.
    Alper CA, Awdeh Z, Raum D, Yunis EJ.
    Biochem Soc Symp; 1986 Dec 22; 51():19-28. PubMed ID: 3493006
    [Abstract] [Full Text] [Related]

  • 18. HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.
    White PC, New MI, Dupont B.
    Proc Natl Acad Sci U S A; 1984 Dec 22; 81(23):7505-9. PubMed ID: 6334310
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  • 20. Genetic polymorphisms of HLA class III and GLO1 in Chinese Yao nationality.
    Wang C, Tian YW, Wu XW, Zhao XZ.
    Gene Geogr; 1990 Apr 22; 4(1):29-34. PubMed ID: 2278900
    [Abstract] [Full Text] [Related]

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