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 *

146 related articles for article (PubMed ID: 1605197)

  • 21. DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity.
    Brown WT; Gross AC; Chan CB; Jenkins EC
    Am J Med Genet; 1986; 23(1-2):643-64. PubMed ID: 3006490
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.
    Ritchie RJ; Knight SJ; Hirst MC; Grewal PK; Bobrow M; Cross GS; Davies KE
    Hum Mol Genet; 1994 Dec; 3(12):2115-21. PubMed ID: 7881407
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular characterization of a DNA probe, U6.2, located close to the fragile X locus.
    Pergolizzi R; Brown WT; Goonewardena P; Bhan R; Dobkin C; Dahl N; Pettersson U
    Am J Med Genet; 1991; 38(2-3):380-3. PubMed ID: 1673315
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Haplotype analysis at the FRAXA locus in the Japanese population.
    Richards RI; Kondo I; Holman K; Yamauchi M; Seki N; Kishi K; Staples A; Sutherland GR; Hori T
    Am J Med Genet; 1994 Jul; 51(4):412-6. PubMed ID: 7943009
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.
    Snow K; Tester DJ; Kruckeberg KE; Schaid DJ; Thibodeau SN
    Hum Mol Genet; 1994 Sep; 3(9):1543-51. PubMed ID: 7833909
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.
    Knight SJ; Flannery AV; Hirst MC; Campbell L; Christodoulou Z; Phelps SR; Pointon J; Middleton-Price HR; Barnicoat A; Pembrey ME
    Cell; 1993 Jul; 74(1):127-34. PubMed ID: 8334699
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.
    Veenema H; Carpenter NJ; Bakker E; Hofker MH; Ward AM; Pearson PL
    J Med Genet; 1987 Jul; 24(7):413-21. PubMed ID: 2886667
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome.
    Thibodeau SN; Dorkins HR; Faulk KR; Berry R; Smith AC; Hagerman R; King A; Davies KE
    Hum Genet; 1988 Jul; 79(3):219-27. PubMed ID: 3402993
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fragile X syndrome.
    Laxova R
    Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Conservation of CGG region in FMR1 gene in mammals.
    Deelen W; Bakker C; Halley DJ; Oostra BA
    Am J Med Genet; 1994 Jul; 51(4):513-6. PubMed ID: 7943032
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probe.
    van Oost BA; Smits AP; Dreesen JC; van den Ouweland AM; Oostra BA
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):320-7. PubMed ID: 1605205
    [TBL] [Abstract][Full Text] [Related]  

  • 32. An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis.
    Forster-Gibson CJ; Mulligan LM; Simpson NE; White BN; Holden JJ
    Am J Med Genet; 1986; 23(1-2):665-83. PubMed ID: 3006491
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Further evidence for genetic heterogeneity in the fragile X syndrome.
    Brown WT; Jenkins EC; Gross AC; Chan CB; Krawczun MS; Duncan CJ; Sklower SL; Fisch GS
    Hum Genet; 1987 Apr; 75(4):311-21. PubMed ID: 2883105
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Instability of the CGG repeat at the FRAXA locus and variable phenotypic expression in a large fragile X pedigree.
    Pintado E; de Diego Y; Hmadcha A; Carrasco M; Sierra J; Lucas M
    J Med Genet; 1995 Nov; 32(11):907-8. PubMed ID: 8592340
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications.
    Forster-Gibson CJ; Mulligan LM; Partington MW; Simpson NE; Holden JJ; White BN
    J Neurogenet; 1985 Jun; 2(3):231-7. PubMed ID: 3860635
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.
    Parrish JE; Oostra BA; Verkerk AJ; Richards CS; Reynolds J; Spikes AS; Shaffer LG; Nelson DL
    Nat Genet; 1994 Nov; 8(3):229-35. PubMed ID: 7874164
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28.
    Oostra BA; Majoor-Krakauer DF; van Hemel JO; Bakker E; Callen DF; Schmidt M; van Oost BA
    Am J Med Genet; 1991; 38(2-3):332-5. PubMed ID: 1673306
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Recombination of DXS548 (RS46) with the FRAXA locus.
    Dreesen JC; Smits AP; van Oost BA
    Am J Med Genet; 1994 Jul; 51(4):535-7. PubMed ID: 7943036
    [No Abstract]   [Full Text] [Related]  

  • 39. The fragile X syndrome: no evidence for any recent mutations.
    Smits AP; Dreesen JC; Post JG; Smeets DF; de Die-Smulders C; Spaans-van der Bijl T; Govaerts LC; Warren ST; Oostra BA; van Oost BA
    J Med Genet; 1993 Feb; 30(2):94-6. PubMed ID: 8445628
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cytogenetic and molecular analysis of dynamic mutation associated with fragile X syndrome.
    Seki N; Ishikiriyama S; Yamauchi M; Hori T
    Jpn J Genet; 1994 Jun; 69(3):259-67. PubMed ID: 8080657
    [TBL] [Abstract][Full Text] [Related]  

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