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121 related items for PubMed ID: 7504514

  • 1. Regional fine mapping of the beta crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2.
    Bijlsma EK, Delattre O, Juyn JA, Melot T, Westerveld A, Dumanski JP, Thomas G, Hulsebos TJ.
    Genes Chromosomes Cancer; 1993 Oct; 8(2):112-8. PubMed ID: 7504514
    [Abstract] [Full Text] [Related]

  • 2. The beta crystallin genes on human chromosome 22 define a new region of homology with mouse chromosome 5.
    Hulsebos TJ, Jenkins NA, Gilbert DJ, Copeland NG.
    Genomics; 1995 Jan 20; 25(2):574-6. PubMed ID: 7789995
    [Abstract] [Full Text] [Related]

  • 3. Direct assignment of the human beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2.
    Hulsebos TJ, Bijlsma EK, Geurts van Kessel AH, Brakenhoff RH, Westerveld A.
    Cytogenet Cell Genet; 1991 Jan 20; 56(3-4):171-5. PubMed ID: 2055112
    [Abstract] [Full Text] [Related]

  • 4. Localization of the beta A4-crystallin gene (CRYBA4) on human chromosome 22 in the region q11.2-->q13.1.
    van Rens GL, Geurts van Kessel AH, Bloemendal H.
    Cytogenet Cell Genet; 1992 Jan 20; 61(3):180-3. PubMed ID: 1424806
    [Abstract] [Full Text] [Related]

  • 5. Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5.
    Hulsebos TJ, Gilbert DJ, Delattre O, Smink LJ, Dunham I, Westerveld A, Thomas G, Jenkins NA, Copeland NG.
    Genomics; 1995 Oct 10; 29(3):712-8. PubMed ID: 8575764
    [Abstract] [Full Text] [Related]

  • 6. Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataract.
    Bateman JB, von-Bischhoffshaunsen FR, Richter L, Flodman P, Burch D, Spence MA.
    Ophthalmology; 2007 Mar 10; 114(3):425-32. PubMed ID: 17234267
    [Abstract] [Full Text] [Related]

  • 7. Confirmation of assignment of the human alpha 1-crystallin gene (CRYA1) to chromosome 21 with regional localization to q22.3.
    Hawkins JW, Van Keuren ML, Piatigorsky J, Law ML, Patterson D, Kao FT.
    Hum Genet; 1987 Aug 10; 76(4):375-80. PubMed ID: 3610158
    [Abstract] [Full Text] [Related]

  • 8. Mapping the breakpoint of a constitutional translocation on chromosome 22 in a patient with NF2.
    Arai E, Tokino T, Imai T, Inazawa J, Ikeuchi T, Tonomura A, Nakamura Y.
    Genes Chromosomes Cancer; 1993 Apr 10; 6(4):235-8. PubMed ID: 7685627
    [Abstract] [Full Text] [Related]

  • 9. DNA diagnosis of neurofibromatosis 2. Altered coding sequence of the merlin tumor suppressor in an extended pedigree.
    MacCollin M, Mohney T, Trofatter J, Wertelecki W, Ramesh V, Gusella J.
    JAMA; 1993 Nov 17; 270(19):2316-20. PubMed ID: 8230593
    [Abstract] [Full Text] [Related]

  • 10. A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22.
    Kramer P, Yount J, Mitchell T, LaMorticella D, Carrero-Valenzuela R, Lovrien E, Maumenee I, Litt M.
    Genomics; 1996 Aug 01; 35(3):539-42. PubMed ID: 8812489
    [Abstract] [Full Text] [Related]

  • 11. Familial meningioma is not allelic to neurofibromatosis 2.
    Pulst SM, Rouleau GA, Marineau C, Fain P, Sieb JP.
    Neurology; 1993 Oct 01; 43(10):2096-8. PubMed ID: 8413972
    [Abstract] [Full Text] [Related]

  • 12. Characterization of the translocation breakpoint on chromosome 22q12.2 in a patient with neurofibromatosis type 2 (NF2).
    Arai E, Ikeuchi T, Nakamura Y.
    Hum Mol Genet; 1994 Jun 01; 3(6):937-9. PubMed ID: 7951241
    [Abstract] [Full Text] [Related]

  • 13. Neurofibromatosis type 2 appears to be a genetically homogeneous disease.
    Narod SA, Parry DM, Parboosingh J, Lenoir GM, Ruttledge M, Fischer G, Eldridge R, Martuza RL, Frontali M, Haines J.
    Am J Hum Genet; 1992 Sep 01; 51(3):486-96. PubMed ID: 1496982
    [Abstract] [Full Text] [Related]

  • 14. Identification of the human beta A2 crystallin gene (CRYBA2): localization of the gene on human chromosome 2 and of the homologous gene on mouse chromosome 1.
    Hulsebos TJ, Cerosaletti KM, Fournier RE, Sinke RJ, Rocchi M, Marzella R, Jenkins NA, Gilbert DJ, Copeland NG.
    Genomics; 1995 Aug 10; 28(3):543-8. PubMed ID: 7490092
    [Abstract] [Full Text] [Related]

  • 15. The neurofibromatosis type 2 gene is inactivated in schwannomas.
    Twist EC, Ruttledge MH, Rousseau M, Sanson M, Papi L, Merel P, Delattre O, Thomas G, Rouleau GA.
    Hum Mol Genet; 1994 Jan 10; 3(1):147-51. PubMed ID: 8162016
    [Abstract] [Full Text] [Related]

  • 16. Mapping of mouse gamma crystallin genes on chromosome 1.
    Skow LC, Donner ME, Huang SM, Gardner JM, Taylor BA, Beamer WG, Lalley PA.
    Biochem Genet; 1988 Oct 10; 26(9-10):557-70. PubMed ID: 3242494
    [Abstract] [Full Text] [Related]

  • 17. Assignment of human gamma crystallin multigene family to chromosome 2.
    Willard HF, Meakin SO, Tsui LC, Breitman ML.
    Somat Cell Mol Genet; 1985 Sep 10; 11(5):511-6. PubMed ID: 2994242
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  • 20. Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.
    Rouleau GA, Seizinger BR, Wertelecki W, Haines JL, Superneau DW, Martuza RL, Gusella JF.
    Am J Hum Genet; 1990 Feb 10; 46(2):323-8. PubMed ID: 2105641
    [Abstract] [Full Text] [Related]

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