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 *

147 related articles for article (PubMed ID: 6321326)

  • 21. The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.
    Oberlé I; Drayna D; Camerino G; White R; Mandel JL
    Proc Natl Acad Sci U S A; 1985 May; 82(9):2824-8. PubMed ID: 2986139
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Familial appraisal of colorblindness in school children of an Indian population.
    Srikumari CR; Rajanikumari J; Rao TV
    J Hered; 1985; 76(1):69-70. PubMed ID: 3872323
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.
    Connor JM; Pirrit LA; Yates JR; Crossley JA; Imrie SJ; Colgan JM
    J Med Genet; 1987 Jan; 24(1):14-22. PubMed ID: 2879932
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19.
    Donald JA; Wallis SC; Kessling A; Tippett P; Robson EB; Ball S; Davies KE; Scambler P; Berg K; Heiberg A
    Hum Genet; 1985; 69(1):39-43. PubMed ID: 3855405
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Hypoxanthine-guanine phosphoribosyltransferase and deutan colour blindness: the relative positions of their loci on the X-chromosome.
    Emmerson BT; Thompson L; Wallace DC; Spence MA
    Adv Exp Med Biol; 1973; 41():281-3. PubMed ID: 4545479
    [No Abstract]   [Full Text] [Related]  

  • 27. Genetic linkage between X-chromosome markers and bipolar affective illness.
    Baron M; Risch N; Hamburger R; Mandel B; Kushner S; Newman M; Drumer D; Belmaker RH
    Nature; 1987 Mar 19-25; 326(6110):289-92. PubMed ID: 3493438
    [TBL] [Abstract][Full Text] [Related]  

  • 28. RECOMBINATION BETWEEN PROTAN AND DEUTAN GENES; DATA ON THEIR RELATIVE POSITONS IN RESPECT OF THE G6PD LOCUS.
    SINISCALCO M; FILIPPI G; LATTE B
    Nature; 1964 Dec; 204():1062-4. PubMed ID: 14243382
    [No Abstract]   [Full Text] [Related]  

  • 29. X mapping in man: evidence against direct measurable linkage between ocular albinism and deutan colour blindness.
    Pearce WG; Sanger R
    J Med Genet; 1976 Aug; 13(4):319. PubMed ID: 1085370
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq.
    Buchanan JA; Buckton KE; Gosden CM; Newton MS; Clayton JF; Christie S; Hastie N
    Hum Genet; 1987 Jun; 76(2):165-72. PubMed ID: 3038730
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.
    Bleeker-Wagemakers LM; Friedrich U; Gal A; Wienker TF; Warburg M; Ropers HH
    Hum Genet; 1985; 71(3):211-4. PubMed ID: 2998969
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome.
    Brown CS; Pearson PL; Thomas NS; Sarfarazi M; Harper PS; Shaw DJ
    J Med Genet; 1985 Jun; 22(3):179-81. PubMed ID: 2989525
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction.
    Greer WL; Mahtani MM; Kwong PC; Rubin LA; Peacocke M; Willard HF; Siminovitch KA
    Hum Genet; 1989 Oct; 83(3):227-30. PubMed ID: 2571560
    [TBL] [Abstract][Full Text] [Related]  

  • 34. New families, one with two recombinants for estimation of recombination between the deutan and protan loci.
    Arias S; Rodríguez A
    Humangenetik; 1972; 14(4):264-8. PubMed ID: 4538150
    [No Abstract]   [Full Text] [Related]  

  • 35. [Heredity of congenital deficiencies in color vision].
    François J; De Bie S; Verriest G; Matton MT
    Acta Genet Med Gemellol (Roma); 1972 Jul; 21(3):233-56. PubMed ID: 4592447
    [No Abstract]   [Full Text] [Related]  

  • 36. X chromosome linkage studies in familial Rett syndrome.
    Curtis AR; Headland S; Lindsay S; Thomas NS; Boye E; Kamakari S; Roustan P; Anvret M; Wahlstrom J; McCarthy G
    Hum Genet; 1993 Jan; 90(5):551-5. PubMed ID: 8094068
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Xq28: epidemiology and sex-linkage between red-green colour blindness and G6PD deficiency.
    Chan YK; Tay MT; Lim MK
    Ann Acad Med Singap; 1992 May; 21(3):318-22. PubMed ID: 1416777
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Isolation and regional mapping of random X sequences from distal human X chromosome.
    Murphy PD; Ruddle FH
    Somat Cell Mol Genet; 1985 Sep; 11(5):433-44. PubMed ID: 2994237
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy.
    Hofker MH; Wapenaar MC; Goor N; Bakker E; van Ommen GJ; Pearson PL
    Hum Genet; 1985; 70(2):148-56. PubMed ID: 2989153
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28.
    Bhattacharya SS; Wright AF; Clayton JF; Price WH; Phillips CI; McKeown CM; Jay M; Bird AC; Pearson PL; Southern EM
    Nature; 1984 May 17-23; 309(5965):253-5. PubMed ID: 6325945
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.