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 *

101 related articles for article (PubMed ID: 3927853)

  • 1. Investigations of chromosomal stability in the Gorlin-Goltz syndrome.
    Römke C; Gödde-Salz E; Grote W
    Arch Dermatol Res; 1985; 277(5):370-2. PubMed ID: 3927853
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndrome.
    Bale AE; Bale SJ; Murli H; Ivett J; Mulvihill JJ; Parry DM
    Cancer Genet Cytogenet; 1989 Oct; 42(2):273-9. PubMed ID: 2507127
    [TBL] [Abstract][Full Text] [Related]  

  • 3. No evidence of chromosomal instability in nevoid basal-cell carcinoma syndrome.
    Sarto F; Mazzotti D; Tomanin R; Corsi GC; Peserico A
    Mutat Res; 1989; 225(1-2):21-6. PubMed ID: 2492367
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Dermatoglyphics and basal cell nevus syndrome (Gorlin-Goltz syndrome)].
    Linss G; Seidlitz G; Schielinsky C
    Dermatol Monatsschr; 1983; 169(10):652-7. PubMed ID: 6642031
    [No Abstract]   [Full Text] [Related]  

  • 5. Evidence of chromosomal instability in the lymphocytes of Gorlin basal-cell carcinoma patients.
    Shafei-Benaissa E; Savage JR; Papworth D; Babin P; Larrègue M; Tanzer J; Bonnetblanc JM; Vaillant L; Huret JL
    Mutat Res; 1995 Nov; 332(1-2):27-32. PubMed ID: 7500988
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Study of basal cell nevus syndrome fibroblasts after treatment with DNA-damaging agents.
    Nagasawa H; Little FF; Burke MJ; McCone EF; Targovnik HS; Chan GL; Little JB
    Basic Life Sci; 1984; 29 Pt B():775-85. PubMed ID: 6442144
    [No Abstract]   [Full Text] [Related]  

  • 7. The naevoid basal-cell carcinoma syndrome (Gorlin syndrome) is a chromosomal instability syndrome.
    Shafei-Benaissa E; Savage JR; Babin P; Larrègue M; Papworth D; Tanzer J; Bonnetblanc JM; Huret JL
    Mutat Res; 1998 Feb; 397(2):287-92. PubMed ID: 9541654
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Gorlin-Goltz syndrome].
    Cesteleyn L; Wierich W
    Z Stomatol; 1984 Jun; 81(3):149-64. PubMed ID: 6591668
    [No Abstract]   [Full Text] [Related]  

  • 9. Familial polyposis coli: no evidence for increased sensitivity to mitomycin C.
    Mazzullo HA; Attwood J; Delhanty JD
    J Med Genet; 1988 Apr; 25(4):233-7. PubMed ID: 2835481
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Checks for chromosomal instability in Gorlin and non-Gorlin basal-cell carcinoma patients.
    Shafei-Benaissa E; Huret JL; Larrègue M; Babin P; Tanzer J; Decrozailles JM; Savage JR
    Mutat Res; 1994 Jul; 308(1):1-9. PubMed ID: 7516477
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The effect of fluoride on chromosome aberration and sister-chromatid exchange frequencies in cultured human lymphocytes.
    Thomson EJ; Kilanowski FM; Perry PE
    Mutat Res; 1985 Oct; 144(2):89-92. PubMed ID: 3930955
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Naevobasaliomatosis (Gorlin-Goltz syndrome)].
    Linss G; Schielinsky C; Schade K; Schmollack E; Knapp A
    Z Arztl Fortbild (Jena); 1979 Dec; 73(24):1163-5. PubMed ID: 551607
    [No Abstract]   [Full Text] [Related]  

  • 13. [Multiple basaloid follicular hamartomas in 2 members of a family with Gorlin-Goltz syndrome].
    Gartmann H; Groth W; Quinkler C
    Z Hautkr; 1989 Oct; 64(10):915-8. PubMed ID: 2588752
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosome-specific patterns of mitomycin C-induced rearrangements in human lymphocytes.
    Schaap T; Sagi M; Cohen MM
    Cytogenet Cell Genet; 1980; 28(4):240-50. PubMed ID: 7460625
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Basal cell carcinoma of the eyelid associated with Gorlin-Goltz syndrome.
    Honavar SG; Shields JA; Shields CL; Eagle RC; Demirci H; Mahmood EZ
    Ophthalmology; 2001 Jun; 108(6):1115-23. PubMed ID: 11382639
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sister chromatid exchange evaluation as an aid to the diagnosis and exclusion of Fanconi's anaemia by induced chromosome damage analysis.
    Howell RT
    J Med Genet; 1991 Jul; 28(7):468-71. PubMed ID: 1910092
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [The HLA system and nevobasaliomatosis (Gorlin-Goltz syndrome)].
    Linss G; Schielinsky C; Schmidt G
    Dermatol Monatsschr; 1981 Jun; 167(6):377-9. PubMed ID: 7274501
    [No Abstract]   [Full Text] [Related]  

  • 18. [Gorlin-Goltz syndrome. Report of a familial case].
    López Haro ML; Garduño Estrada R; Alcántar R
    Rev ADM; 1988; 45(2):81-6. PubMed ID: 3251512
    [No Abstract]   [Full Text] [Related]  

  • 19. [Gorlin-Goltz syndrome].
    Gyenes V; Pataky L; Csiba A
    Orv Hetil; 1981 Aug; 122(32):1967-9. PubMed ID: 7301365
    [No Abstract]   [Full Text] [Related]  

  • 20. Sister chromatid exchange distribution in bone marrow cell chromosomes from patients with refractory anemia.
    Carbone P; Barbata G; Granata G; Margiotta G; Caronia F
    Acta Haematol; 1981; 65(3):177-82. PubMed ID: 6785971
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.