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Journal Abstract Search

233 related items for PubMed ID: 2912884

  • 1. Localization of Y chromosome sequences and X chromosomal replication studies in XX males.
    Schempp W, Müller G, Scherer G, Bohlander SK, Rommerskirch W, Fraccaro M, Wolf U.
    Hum Genet; 1989 Jan; 81(2):144-8. PubMed ID: 2912884
    [Abstract] [Full Text] [Related]

  • 2. Steroid sulfatase gene in XX males.
    Mohandas TK, Stern HJ, Meeker CA, Passage MB, Müller U, Page DC, Yen PH, Shapiro LJ.
    Am J Hum Genet; 1990 Feb; 46(2):369-76. PubMed ID: 2301402
    [Abstract] [Full Text] [Related]

  • 3. A comparative study on steroid sulfatase and arylsulfatase C in fibroblast clones from 45,X/47,XXX and 69,XXY.
    Vogel W, Grompe M, Storz R, Pentz S.
    Hum Genet; 1984 Feb; 66(4):367-9. PubMed ID: 6586638
    [Abstract] [Full Text] [Related]

  • 4. [Study on the steroid sulfatase (STS) activity in normal individuals and patients with abnormal sexual differentiation].
    Shinohara M.
    Nihon Naibunpi Gakkai Zasshi; 1989 Mar 20; 65(3):161-73. PubMed ID: 2767285
    [Abstract] [Full Text] [Related]

  • 5. Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.
    Ballabio A, Parenti G, Carrozzo R, Sebastio G, Andria G, Buckle V, Fraser N, Craig I, Rocchi M, Romeo G.
    Proc Natl Acad Sci U S A; 1987 Jul 20; 84(13):4519-23. PubMed ID: 3474618
    [Abstract] [Full Text] [Related]

  • 6. Y-specific DNA sequences in male patients with 46,XX and 47,XXX karyotypes.
    Müller U, Latt SA, Donlon T.
    Am J Med Genet; 1987 Oct 20; 28(2):393-401. PubMed ID: 2827475
    [Abstract] [Full Text] [Related]

  • 7. Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene?
    Fraser N, Ballabio A, Zollo M, Persico G, Craig I.
    Development; 1987 Oct 20; 101 Suppl():127-32. PubMed ID: 3503710
    [Abstract] [Full Text] [Related]

  • 8. Activity of steroid sulfatase in fibroblasts with numerical and structural X chromosome aberrations.
    Ropers HH, Migl B, Zimmer J, Fraccaro M, Maraschio PP, Westerveld A.
    Hum Genet; 1981 Oct 20; 57(4):354-6. PubMed ID: 6945285
    [Abstract] [Full Text] [Related]

  • 9. An unusual case of X-15 translocation: evidence for the presence of an 'activator' region on Xpter of man.
    Crocker M, Jonasson J, Patel C.
    Clin Genet; 1985 Dec 20; 28(6):556-60. PubMed ID: 3865752
    [Abstract] [Full Text] [Related]

  • 10. Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals.
    Petit C, Levilliers J, Rouyer F, Simmler MC, Herouin E, Weissenbach J.
    Genomics; 1990 Apr 20; 6(4):651-8. PubMed ID: 2341154
    [Abstract] [Full Text] [Related]

  • 11. Pericentric inversion of the X chromosome: presentation of a case and review of the literature.
    Schorderet DF, Friedman C, Disteche CM.
    Ann Genet; 1991 Apr 20; 34(2):98-103. PubMed ID: 1746892
    [Abstract] [Full Text] [Related]

  • 12. Isolation of a new gene from the distal short arm of the human X chromosome that escapes X-inactivation.
    Yen PH, Ellison J, Salido EC, Mohandas T, Shapiro L.
    Hum Mol Genet; 1992 Apr 20; 1(1):47-52. PubMed ID: 1284467
    [Abstract] [Full Text] [Related]

  • 13. Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency).
    Gillard EF, Affara NA, Yates JR, Goudie DR, Lambert J, Aitken DA, Ferguson-Smith MA.
    Nucleic Acids Res; 1987 May 26; 15(10):3977-85. PubMed ID: 2884621
    [Abstract] [Full Text] [Related]

  • 14. Physical mapping of loci in the distal half of the short arm of the human X chromosome: implications for the spreading of X-chromosome inactivation.
    Wang JC, Passage MB, Ellison J, Becker MA, Yen PH, Shapiro LJ, Mohandas TK.
    Somat Cell Mol Genet; 1992 Mar 26; 18(2):195-200. PubMed ID: 1315458
    [Abstract] [Full Text] [Related]

  • 15. Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism.
    Fechner PY, Rosenberg C, Stetten G, Cargile CB, Pearson PL, Smith KD, Migeon CJ, Berkovitz GD.
    Cytogenet Cell Genet; 1994 Mar 26; 66(1):22-6. PubMed ID: 8275702
    [Abstract] [Full Text] [Related]

  • 16. Molecular studies of deletions at the human steroid sulfatase locus.
    Shapiro LJ, Yen P, Pomerantz D, Martin E, Rolewic L, Mohandas T.
    Proc Natl Acad Sci U S A; 1989 Nov 26; 86(21):8477-81. PubMed ID: 2813406
    [Abstract] [Full Text] [Related]

  • 17. Cytogenetic and molecular studies on a recombinant human X chromosome: implications for the spreading of X chromosome inactivation.
    Mohandas T, Geller RL, Yen PH, Rosendorff J, Bernstein R, Yoshida A, Shapiro LJ.
    Proc Natl Acad Sci U S A; 1987 Jul 26; 84(14):4954-8. PubMed ID: 3474636
    [Abstract] [Full Text] [Related]

  • 18. Isolation and characterization of a yeast artificial chromosome (YAC) contig around the human steroid sulfatase gene.
    Carrozzo R, Ellison J, Yen P, Taillon-Miller P, Brownstein BH, Persico G, Ballabio A, Shapiro L.
    Genomics; 1992 Jan 26; 12(1):7-12. PubMed ID: 1733866
    [Abstract] [Full Text] [Related]

  • 19. Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: implications for X-Y interchange.
    Yen PH, Allen E, Marsh B, Mohandas T, Wang N, Taggart RT, Shapiro LJ.
    Cell; 1987 May 22; 49(4):443-54. PubMed ID: 3032454
    [Abstract] [Full Text] [Related]

  • 20. A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.
    Koenig M, Camerino G, Heilig R, Mandel JL.
    Nucleic Acids Res; 1984 May 25; 12(10):4097-109. PubMed ID: 6728677
    [Abstract] [Full Text] [Related]

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