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 *

153 related articles for article (PubMed ID: 3482420)

  • 41. No genetic linkage detected for schizophrenia to Xq27-q28.
    Delisi LE; Crow TJ; Davies KE; Terwilliger JD; Ott J; Ram R; Flint T; Boccio A
    Br J Psychiatry; 1991 May; 158():630-4. PubMed ID: 1677599
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivation.
    Marshall LS; Simon J; Wood T; Peng M; Owen R; Feldman GS; Zaragoza MV
    BMC Med Genet; 2013 May; 14():49. PubMed ID: 23634718
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Linkage homogeneity near the fragile X locus in normal and fragile X families.
    Suthers GK; Mulley JC; Voelckel MA; Dahl N; Väisänen ML; Steinbach P; Glass IA; Schwartz CE; van Oost BA; Thibodeau SN
    Genomics; 1991 Jul; 10(3):576-82. PubMed ID: 1889808
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.
    Schwartz C; Fitch N; Phelan MC; Richer CL; Stevenson R
    Hum Genet; 1987 May; 76(1):54-7. PubMed ID: 3471705
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Localisation of the gene for Hunter syndrome on the long arm of X chromosome.
    Upadhyaya M; Sarfarazi M; Bamforth JS; Thomas NS; Oberle I; Young I; Harper PS
    Hum Genet; 1986 Dec; 74(4):391-8. PubMed ID: 2878868
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers.
    Glass IA; Pirrit LA; White EM; Bell MV; Davies KE; Cockburn F; Connor JM
    Am J Med Genet; 1991; 38(2-3):298-304. PubMed ID: 1673301
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.
    Patterson M; Kenwrick S; Thibodeau S; Faulk K; Mattei MG; Mattei JF; Davies KE
    Nucleic Acids Res; 1987 Mar; 15(6):2639-51. PubMed ID: 2882476
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia.
    Schwartz M; Yang HM; Niebuhr E; Rosenberg T; Page DC
    Hum Genet; 1988 Feb; 78(2):156-60. PubMed ID: 3422216
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males.
    Winter RM; Pembrey ME
    Hum Genet; 1986 Sep; 74(1):93-7. PubMed ID: 3463533
    [TBL] [Abstract][Full Text] [Related]  

  • 50. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P; Dahl N; Gustavson KH; Holmgren G; Pettersson U
    Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Microdissection of the fragile X region.
    MacKinnon RN; Hirst MC; Bell MV; Watson JE; Claussen U; Ludecke HJ; Senger G; Horsthemke B; Davies KE
    Am J Hum Genet; 1990 Aug; 47(2):181-6. PubMed ID: 2378345
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.
    Mattei MG; Baeteman MA; Heilig R; Oberlé I; Davies K; Mandel JL; Mattei JF
    Hum Genet; 1985; 69(4):327-31. PubMed ID: 2985491
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.
    Richards RI; Shen Y; Holman K; Kozman H; Hyland VJ; Mulley JC; Sutherland GR
    Am J Hum Genet; 1991 Jun; 48(6):1051-7. PubMed ID: 2035525
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Increase in the incidence of the fragile site Xq27 in prometaphases.
    Barbi G; Steinbach P
    Hum Genet; 1982; 61(1):82. PubMed ID: 6957373
    [No Abstract]   [Full Text] [Related]  

  • 55. Long-range restriction map of the terminal part of the short arm of the human X chromosome.
    Petit C; Levilliers J; Weissenbach J
    Proc Natl Acad Sci U S A; 1990 May; 87(10):3680-4. PubMed ID: 2339111
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Frequency of the common fragile site at Xq27.2 under conditions of thymidylate stress: implications for cytogenetic diagnosis of the fragile-X syndrome.
    Ramos FJ; Emanuel BS; Spinner NB
    Am J Med Genet; 1992 Apr; 42(6):835-8. PubMed ID: 1532475
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.
    Brown WT; Ye W; Gross AC; Chan CB; Dobkin CS; Jenkins EC
    Am J Med Genet; 1988; 30(1-2):551-66. PubMed ID: 2902796
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. Fragile X syndrome and nephrogenic diabetes insipidus.
    Suthers GK; Turner G; Mulley JC
    Am J Med Genet; 1988; 30(1-2):231-6. PubMed ID: 3177449
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A radiation hybrid map of the proximal short arm of the human X chromosome spanning incontinentia pigmenti 1 (IP1) translocation breakpoints.
    Gorski JL; Boehnke M; Reyner EL; Burright EN
    Genomics; 1992 Nov; 14(3):657-65. PubMed ID: 1427892
    [TBL] [Abstract][Full Text] [Related]  

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