BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (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
    [TBL] [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; 25(2):574-6. PubMed ID: 7789995
    [TBL] [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; 56(3-4):171-5. PubMed ID: 2055112
    [TBL] [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; 61(3):180-3. PubMed ID: 1424806
    [TBL] [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; 29(3):712-8. PubMed ID: 8575764
    [TBL] [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; 114(3):425-32. PubMed ID: 17234267
    [TBL] [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; 76(4):375-80. PubMed ID: 3610158
    [TBL] [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; 6(4):235-8. PubMed ID: 7685627
    [TBL] [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; 270(19):2316-20. PubMed ID: 8230593
    [TBL] [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; 35(3):539-42. PubMed ID: 8812489
    [TBL] [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; 43(10):2096-8. PubMed ID: 8413972
    [TBL] [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; 3(6):937-9. PubMed ID: 7951241
    [TBL] [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; 51(3):486-96. PubMed ID: 1496982
    [TBL] [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; 28(3):543-8. PubMed ID: 7490092
    [TBL] [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; 3(1):147-51. PubMed ID: 8162016
    [TBL] [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; 26(9-10):557-70. PubMed ID: 3242494
    [TBL] [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; 11(5):511-6. PubMed ID: 2994242
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
    Bateman JB; Geyer DD; Flodman P; Johannes M; Sikela J; Walter N; Moreira AT; Clancy K; Spence MA
    Invest Ophthalmol Vis Sci; 2000 Oct; 41(11):3278-85. PubMed ID: 11006214
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus.
    Sanson M; Marineau C; Desmaze C; Lutchman M; Ruttledge M; Baron C; Narod S; Delattre O; Lenoir G; Thomas G
    Hum Mol Genet; 1993 Aug; 2(8):1215-20. PubMed ID: 8401504
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 46(2):323-8. PubMed ID: 2105641
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.