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Journal Abstract Search

121 related items for PubMed ID: 692595

  • 1. Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group.
    Levine LS, Zachmann M, New MI, Prader A, Pollack MS, O'Neill GJ, Yang SY, Oberfield SE, Dupont B.
    N Engl J Med; 1978 Oct 26; 299(17):911-5. PubMed ID: 692595
    [Abstract] [Full Text] [Related]

  • 2. Mapping of the 21-hydroxylase deficiency gene within the HLA linkage group.
    Yang SY, Levine LS, Zachmann M, New MI, Prader A, Oberfield SE, O'Neill GJ, Pollack MS, Dupont B.
    Transplant Proc; 1978 Dec 26; 10(4):753-5. PubMed ID: 734746
    [No Abstract] [Full Text] [Related]

  • 3. Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).
    Dupont B, Oberfield SE, Smithwick EM, Lee TD, Levine LS.
    Lancet; 1978 Dec 26; 2(8052-8053):1309-12. PubMed ID: 74726
    [Abstract] [Full Text] [Related]

  • 4. Intelligence of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency, their parents and unaffected siblings.
    Wenzel U, Schneider M, Zachmann M, Knorr-Mürset G, Weber A, Prader A.
    Helv Paediatr Acta; 1978 Apr 26; 33(1):11-6. PubMed ID: 669967
    [Abstract] [Full Text] [Related]

  • 5. Possible genetic linkage disequilibrium between HLA and the 21-hydroxylase deficiency gene (congenital adrenal hyperplasia).
    Pollack MS, Levine L, Zachmann M, Prader A, New M, Oberfield S, Dupont B.
    Transplant Proc; 1979 Jun 26; 11(2):1315-6. PubMed ID: 314176
    [No Abstract] [Full Text] [Related]

  • 6. Investigations of red cell glyoxalase in recombinant families.
    Pretorius AM, Scholz S, Kuntz B, Albert ED.
    Eur J Immunol; 1976 Oct 26; 6(10):759-61. PubMed ID: 1015713
    [Abstract] [Full Text] [Related]

  • 7. The chromosomal order of genes controlling the major histocompatibility complex, properdin factor B, and deficiency of the second component of complement.
    Raum D, Glass D, Carpenter CB, Alper CA, Schur PH.
    J Clin Invest; 1976 Nov 26; 58(5):1240-8. PubMed ID: 993342
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of congenital adrenal hyperplasia.
    Marcus ES, Holcombe JH, Tulchinsky D, Rich RR, Riccardi VM.
    Am J Med Genet; 1979 Nov 26; 4(2):201-4. PubMed ID: 517576
    [Abstract] [Full Text] [Related]

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  • 10. Genetic linkage of a locus for erythrocyte glyoxalase (GLO) with HLA and Bf.
    Weitkamp LR, Guttormsen SA.
    Birth Defects Orig Artic Ser; 1976 Nov 26; 12(7):364-6. PubMed ID: 1024642
    [No Abstract] [Full Text] [Related]

  • 11. Linkage of human narcolepsy with HLA association to chromosome 4p13-q21.
    Nakayama J, Miura M, Honda M, Miki T, Honda Y, Arinami T.
    Genomics; 2000 Apr 01; 65(1):84-6. PubMed ID: 10777671
    [Abstract] [Full Text] [Related]

  • 12. The locus for glyoxalase I (GLO) is between HLA-A and PGM3 on chromosome 6 of man.
    Meera Khan P, Volkers WS, Doppert BA, Bijnen AB, Schreuder I, Van Rood JJ.
    Birth Defects Orig Artic Ser; 1976 Apr 01; 12(7):328-30. PubMed ID: 1024634
    [No Abstract] [Full Text] [Related]

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  • 14. Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing.
    Jackson JF, Currier RD, Terasaki PI, Morton NE.
    N Engl J Med; 1977 May 19; 296(20):1138-41. PubMed ID: 857157
    [Abstract] [Full Text] [Related]

  • 15. HLA and congenital adrenal hyperplasia linkage confirmed.
    Lancet; 1978 Apr 29; 1(8070):930-2. PubMed ID: 76861
    [No Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing.
    Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon M, Owens RP, Merkatz IR, Nitowsky BM, Sachs G, Dupont B.
    Lancet; 1979 May 26; 1(8126):1107-8. PubMed ID: 86832
    [Abstract] [Full Text] [Related]

  • 17. HLA antigens and acute rheumatic fever: evidence for a recessive susceptibility gene linked to HLA.
    Hafez M, Chakravarti A, el-Shennawy F, el-Morsi Z, el-Sallab SH, Al-Tonbary Y.
    Genet Epidemiol; 1985 May 26; 2(3):273-82. PubMed ID: 4054602
    [Abstract] [Full Text] [Related]

  • 18. Linkage analysis between the major histocompatibility system and insulin-dependent diabetes in families with patients in two consecutive generations.
    Barbosa J, Chern MM, Anderson VE, Noreen H, Johnson S, Reinsmoen N, McCarty R, King R, Greenberg L.
    J Clin Invest; 1980 Mar 26; 65(3):592-601. PubMed ID: 6766467
    [Abstract] [Full Text] [Related]

  • 19. Diagnosis of classical steroid 21-hydroxylase deficiency using an HLA-B locus-specific DNA-probe.
    Killeen AA, Seelig S, Ulstrom RA, Orr HT.
    Am J Med Genet; 1988 Mar 26; 29(3):703-12. PubMed ID: 2897792
    [Abstract] [Full Text] [Related]

  • 20. Possible linkage of a breast cancer-susceptibility locus to the ABO locus: sensitivity of LOD scores to a single new recombinant observation.
    Skolnick MH, Thompson EA, Bishop DT, Cannon LA.
    Genet Epidemiol; 1984 Mar 26; 1(4):363-73. PubMed ID: 6544244
    [Abstract] [Full Text] [Related]

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