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 *

99 related articles for article (PubMed ID: 7835091)

  • 1. Fine deletion mapping of the p22 region of the human X chromosome using a radiation-induced hybrid panel.
    Heuertz S; Smahi A; Sanak M; Holvoet-Vermaut L; Hors-Cayla MC
    Cytogenet Cell Genet; 1995; 69(1-2):7-10. PubMed ID: 7835091
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene.
    Biancalana V; Trivier E; Weber C; Weissenbach J; Rowe PS; O'Riordan JL; Partington MW; Heyberger S; Oudet C; Hanauer A
    Genomics; 1994 Aug; 22(3):617-25. PubMed ID: 8001973
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region.
    Alitalo T; Kruse TA; Ahrens P; Albertsen HM; Eriksson AW; de la Chapelle A
    Hum Genet; 1991 Apr; 86(6):599-603. PubMed ID: 1673960
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Deletion mapping and a highly reduced radiation hybrid in the Xp22.3-p22.2 region.
    Schnur RE; Wick PA; Sosnoski DN; Bick D; Nussbaum RL
    Genomics; 1993 Mar; 15(3):500-6. PubMed ID: 8468044
    [TBL] [Abstract][Full Text] [Related]  

  • 5. X-linked juvenile retinoschisis: localization between (DXS1195, DXS418) and AFM291wf5 on a single YAC.
    Pawar H; Bingham EL; Hiriyanna K; Segal M; Richards JE; Sieving PA
    Hum Hered; 1996; 46(6):329-35. PubMed ID: 8956029
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes.
    Alitalo T; Francis F; Kere J; Lehrach H; Schlessinger D; Willard HF
    Genomics; 1995 Feb; 25(3):691-700. PubMed ID: 7759104
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An irradiation-reduced hybrid panel for fine-structure mapping of the Xq28 region in the human genome.
    Peterlin B; Smahi A; Holvoet-Vermaut L; Heitz D; Dahl N; Hors-Cayla MC
    Cytogenet Cell Genet; 1993; 62(1):58-9. PubMed ID: 8422759
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region.
    Toutain A; Ronce N; Dessay B; Robb L; Francannet C; Le Merrer M; Briard ML; Kaplan J; Moraine C
    Hum Genet; 1997 Feb; 99(2):256-61. PubMed ID: 9048931
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Refined localization of the gene causing X-linked juvenile retinoschisis.
    Alitalo T; Kruse TA; de la Chapelle A
    Genomics; 1991 Mar; 9(3):505-10. PubMed ID: 2032721
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The gene for spondyloepiphyseal dysplasia (SEDL) maps to Xp22 between DXS16 and DXS92.
    Heuertz S; Nelen M; Wilkie AO; Le Merrer M; Delrieu O; Larget-Piet L; Tranebjaerg L; Bick D; Hamel B; Van Oost BA
    Genomics; 1993 Oct; 18(1):100-4. PubMed ID: 7903956
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families.
    Thakker RV; Davies KE; Read AP; Tippett P; Wooding C; Flint T; Wood S; Kruse TA; Whyte MP; O'Riordan JL
    Genomics; 1990 Oct; 8(2):189-93. PubMed ID: 1979046
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS.
    Van de Vosse E; Bergen AA; Meershoek EJ; Oosterwijk JC; Gregory S; Bakker B; Weissenbach J; Coffey AJ; van Ommen GJ; Den Dunnen JT
    Eur J Hum Genet; 1996; 4(2):101-4. PubMed ID: 8744027
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease gene.
    Oudet C; Weber C; Kaplan J; Segues B; Croquette MF; Roman EO; Hanauer A
    J Med Genet; 1993 Apr; 30(4):300-3. PubMed ID: 8487275
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysis.
    Hanauer A; Alembik Y; Gilgenkrantz S; Mujica P; Nivelon-Chevallier A; Pembrey ME; Young ID; Mandel JL
    Am J Med Genet; 1988; 30(1-2):523-30. PubMed ID: 3177469
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Use of Alu-PCR to characterize hybrids containing multiple fragments and to generate new Xp21.3-p22.2 markers.
    Benham F; Rowe P
    Genomics; 1992 Feb; 12(2):368-76. PubMed ID: 1740346
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome.
    Brown CJ; Mahtani MM; Willard HF
    Hum Genet; 1988 Nov; 80(3):296-8. PubMed ID: 3192218
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry.
    Schnur RE; Trask BJ; van den Engh G; Punnett HH; Kistenmacher M; Tomeo MA; Naids RE; Nussbaum RL
    Am J Hum Genet; 1989 Nov; 45(5):706-20. PubMed ID: 2573275
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22.
    Thiselton DL; Lindsay S; Kamakari S; Hardcastle AJ; Roustan P; Bhattacharya SS
    Genomics; 1995 Jan; 25(1):279-81. PubMed ID: 7774929
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 6(4):651-8. PubMed ID: 2341154
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Radiation hybrids for the proximal long arm of the X chromosome and their use in the derivation of an ordered set of cosmid markers from a defined subregion in proximal Xq13.1.
    Röhme D; Sidén T; van der Maarel SM; Cremers FP; Tantravahi U; Marinoni JC; Ropers HH; Schwartz CE
    Somat Cell Mol Genet; 1994 Jan; 20(1):1-10. PubMed ID: 8197472
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.