These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 2571578)

  • 1. Large-scale mapping and chromosome jumping in the q27 region of the human X chromosome.
    Nguyen C; Poustka AM; Djabali M; Roux D; Mattei JF; Lehrach H; Jordan BR
    Genomics; 1989 Aug; 5(2):298-303. PubMed ID: 2571578
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile site.
    Nguyen C; Mattei MG; Rey JA; Baeteman MA; Mattei JF; Jordan BR
    Am J Med Genet; 1988; 30(1-2):601-11. PubMed ID: 2902799
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkage.
    Faust CJ; Levinson B; Gitschier J; Herman GE
    Genomics; 1992 Aug; 13(4):1289-95. PubMed ID: 1354645
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Toward a physical map of the Xq28 region in man: linking color vision, G6PD, and coagulation factor VIII genes to an X-Y homology region.
    Arveiler B; Vincent A; Mandel JL
    Genomics; 1989 May; 4(4):460-71. PubMed ID: 2501212
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR).
    Kirkilionis AJ; Gregory CA; Hamerton JL
    Genomics; 1991 Mar; 9(3):524-35. PubMed ID: 2032723
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosome jumping from D4S10 (G8) toward the Huntington disease gene.
    Richards JE; Gilliam TC; Cole JL; Drumm ML; Wasmuth JJ; Gusella JF; Collins FS
    Proc Natl Acad Sci U S A; 1988 Sep; 85(17):6437-41. PubMed ID: 2901098
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic and physical mapping of the biglycan gene on the mouse X chromosome.
    Chatterjee A; Faust CJ; Herman GE
    Mamm Genome; 1993; 4(1):33-6. PubMed ID: 8093671
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparison of the physical and recombination maps of the mouse X chromosome.
    Disteche CM; McConnell GK; Grant SG; Stephenson DA; Chapman VM; Gandy S; Adler DA
    Genomics; 1989 Aug; 5(2):177-84. PubMed ID: 2571569
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pulsed-field gradient-gel studies around the fragile site.
    Dobkin CS; Brown WT
    Am J Med Genet; 1988; 30(1-2):593-600. PubMed ID: 2902798
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Physical mapping of the loci Gabra3, DXPas8, CamL1, and Rsvp in a region of the mouse X chromosome homologous to human Xq28.
    Faust CJ; Herman GE
    Genomics; 1991 Sep; 11(1):154-64. PubMed ID: 1684949
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Physical mapping of probes proximal to the fragile X locus (FRAX) confirms the order F9-DXS105 (cX55.7)-DXS98 (4D8)-FRAXA.
    Sauer SM; Phelan MC; Richer CL; Schwartz CE
    Cytogenet Cell Genet; 1989; 50(2-3):172-3. PubMed ID: 2776486
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Physical mapping in the region of human Xq12-21.1 using pulsed field gel electrophoresis.
    Jones AM; Malcolm S; Levinsky RJ; Kinnon C
    Hum Genet; 1993 Jun; 91(5):485-8. PubMed ID: 8314562
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.
    Oberlé I; Camerino G; Wrogemann K; Arveiler B; Hanauer A; Raimondi E; Mandel JL
    Hum Genet; 1987 Sep; 77(1):60-5. PubMed ID: 3502701
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8.
    Iannuzzi MC; Dean M; Drumm ML; Hidaka N; Cole JL; Perry A; Stewart C; Gerrard B; Collins FS
    Am J Hum Genet; 1989 May; 44(5):695-703. PubMed ID: 2565081
    [TBL] [Abstract][Full Text] [Related]  

  • 15. High-density molecular map of the central span of the mouse X chromosome.
    Brockdorff N; Kay G; Smith S; Keer JT; Hamvas RM; Brown SD; Rastan S
    Genomics; 1991 May; 10(1):17-22. PubMed ID: 1675191
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Localization of the mouse Mcf-2 (Dbl) protooncogene within a conserved linkage group on the mouse X chromosome.
    Grant SG; Mattei MG; Galland F; Stephenson DA; Keitz BT; Birnbaum D; Chapman VM
    Cytogenet Cell Genet; 1990; 54(3-4):175-81. PubMed ID: 2265564
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map.
    Higgins MJ; Turmel C; Noolandi J; Neumann PE; Lalande M
    Proc Natl Acad Sci U S A; 1990 May; 87(9):3415-9. PubMed ID: 1970636
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.
    Merry DE; Lesko JG; Sosnoski DM; Lewis RA; Lubinsky M; Trask B; van den Engh G; Collins FS; Nussbaum RL
    Am J Hum Genet; 1989 Oct; 45(4):530-40. PubMed ID: 2491012
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial deletions of a sequence family ("DXS278") and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresis.
    Schnur RE; Knowlton RG; Musarella MA; Muenke M; Nussbaum RL
    Genomics; 1990 Oct; 8(2):255-62. PubMed ID: 1979048
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Physical mapping studies on the human X chromosome in the region Xq27-Xqter.
    Patterson M; Schwartz C; Bell M; Sauer S; Hofker M; Trask B; van den Engh G; Davies KE
    Genomics; 1987 Dec; 1(4):297-306. PubMed ID: 3482420
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.