BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

37 related articles for article (PubMed ID: 3460742)

  • 1. Characterization of chromatin at structurally abnormal inactive X chromosomes reveals potential evidence of a rare hybrid active and inactive isodicentric X chromosome.
    Chadwick BP
    Chromosome Res; 2020 Jun; 28(2):155-169. PubMed ID: 31776830
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
    Greenberg CR; Hamerton JL; Nigli M; Wrogemann K
    Am J Hum Genet; 1987 Aug; 41(2):128-37. PubMed ID: 3475976
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome.
    Szpiro-Tapia S; Sefiani A; Guilloud-Bataille M; Heuertz S; Le Marec B; Frézal J; Maroteaux P; Hors-Cayla MC
    Hum Genet; 1988 Dec; 81(1):61-3. PubMed ID: 3198127
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq.
    Cremers FP; van de Pol TJ; Wieringa B; Hofker MH; Pearson PL; Pfeiffer RA; Mikkelsen M; Tabor A; Ropers HH
    Am J Hum Genet; 1988 Oct; 43(4):452-61. PubMed ID: 3177387
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.
    Zonana J; Clarke A; Sarfarazi M; Thomas NS; Roberts K; Marymee K; Harper PS
    Am J Hum Genet; 1988 Jul; 43(1):75-85. PubMed ID: 3163892
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A DNA marker closely linked to the factor IX (haemophilia B) gene.
    Mulligan L; Holden JJ; White BN
    Hum Genet; 1987 Apr; 75(4):381-3. PubMed ID: 2883108
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Physical fine-mapping of a deletion spanning the Norrie gene.
    Diergaarde PJ; Wieringa B; Bleeker-Wagemakers EM; Sims KB; Breakefield XO; Ropers HH
    Hum Genet; 1989 Dec; 84(1):22-6. PubMed ID: 2606473
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.
    Hyland VJ; Fernandez KE; Callen DF; MacKinnon RN; Baker E; Friend K; Sutherland GR
    Hum Genet; 1989 Aug; 83(1):61-6. PubMed ID: 2570019
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Isolation and mapping of a polymorphic DNA sequence, DXS312, to Xq27----Xq28.
    Mulligan L; Sood R; Poon R; White BN; Holden JJ
    Nucleic Acids Res; 1989 Jun; 17(11):4421. PubMed ID: 2567985
    [No Abstract]   [Full Text] [Related]  

  • 11. Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq.
    Skare JC; Sullivan JL; Milunsky A
    Hum Genet; 1989 Jul; 82(4):349-53. PubMed ID: 2567695
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.
    Schmidt M; Certoma A; Du Sart D; Kalitsis P; Leversha M; Fowler K; Sheffield L; Jack I; Danks DM
    Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Physical mapping of an Xq-proximal interstitial duplication in a male.
    Muscatelli F; Verna JM; Philip N; Moncla A; Mattei MG; Mattei JF; Fontes M
    Hum Genet; 1992 Mar; 88(6):691-4. PubMed ID: 1551675
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Regional localization of 18 human X-linked DNA sequences.
    Riddell DC; Wang HS; Beckett J; Chan A; Holden JJ; Mulligan LM; Phillips MA; Simpson NE; Wrogemann K; Hamerton JL
    Cytogenet Cell Genet; 1986; 42(3):123-8. PubMed ID: 3460742
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.
    de Martinville B; Kunkel LM; Bruns G; Morlé F; Koenig M; Mandel JL; Horwich A; Latt SA; Gusella JF; Housman D
    Am J Hum Genet; 1985 Mar; 37(2):235-49. PubMed ID: 2984924
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolation and analysis of DNA markers specific to human chromosome 15.
    Tasset DM; Hartz JA; Kao FT
    Am J Hum Genet; 1988 Jun; 42(6):854-66. PubMed ID: 2897161
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids.
    Brook JD; Shaw DJ; Thomas NS; Meredith AL; Cowell J; Harper PS
    Cytogenet Cell Genet; 1986; 41(1):30-7. PubMed ID: 3455910
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sex chromosome-specific DNA sequences.
    Davies KE; Taylor P; Müller CR
    Differentiation; 1983; 23 Suppl():S44-7. PubMed ID: 6444174
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Human gene mapping, genetic linkage, and clinical applications.
    Ann Intern Med; 1980 Sep; 93(3):469-79. PubMed ID: 6159813
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 2.