BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 8544194)

  • 1. Genotype-phenotype correlations of new causative APC gene mutations in patients with familial adenomatous polyposis.
    Bunyan DJ; Shea-Simonds J; Reck AC; Finnis D; Eccles DM
    J Med Genet; 1995 Sep; 32(9):728-31. PubMed ID: 8544194
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis.
    Wallis YL; Macdonald F; Hultén M; Morton JE; McKeown CM; Neoptolemos JP; Keighley M; Morton DG
    Hum Genet; 1994 Nov; 94(5):543-8. PubMed ID: 7959691
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutations.
    Valanzano R; Cama A; Volpe R; Curia MC; Mencucci R; Palmirotta R; Battista P; Ficari F; Mariani-Costantini R; Tonelli F
    Cancer; 1996 Dec; 78(11):2400-10. PubMed ID: 8941012
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital hypertrophy of the retinal pigment epithelium and APC mutations in two Chinese families with familial adenomatous polyposis.
    Pang CP; Keung JW; Tang NL; Fan DS; Lau JW; Lam DS
    Eye (Lond); 2000 Feb; 14 ( Pt 1)():18-22. PubMed ID: 10755094
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutations.
    Reck AC; Bunyan D; Eccles D; Humphry R
    Eye (Lond); 1997; 11 ( Pt 3)():298-300. PubMed ID: 9373466
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital hypertrophy of the retinal pigment epithelium and APC mutations in Chinese with familial adenomatous polyposis.
    Pang CP; Fan DS; Keung JW; Baum L; Tang NL; Lau JW; Lam DS
    Ophthalmologica; 2001; 215(6):408-11. PubMed ID: 11741105
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary.
    Papp J; Kovacs ME; Matrai Z; Orosz E; Kásler M; Børresen-Dale AL; Olah E
    Fam Cancer; 2016 Jan; 15(1):85-97. PubMed ID: 26446593
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The most frequent APC mutations among Slovak familial adenomatous polyposis patients. Adenomatous polyposis coli.
    Zajac V; Kovác M; Kirchhoff T; Stevurková V; Tomka M
    Neoplasma; 2002; 49(6):356-61. PubMed ID: 12584582
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Congenital hypertrophy of retinal pigment epithelium: a marker in familial adenomatous polyposis].
    Szwarcberg J; Limacher JM; Fricker JP; Flament J
    J Fr Ophtalmol; 1999 Apr; 22(3):364-70. PubMed ID: 10337595
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fundus lesions of adenomatous polyposis.
    Tiret A; Parc C
    Curr Opin Ophthalmol; 1999 Jun; 10(3):168-72. PubMed ID: 10537774
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): a review of the literature.
    Nieuwenhuis MH; Vasen HF
    Crit Rev Oncol Hematol; 2007 Feb; 61(2):153-61. PubMed ID: 17064931
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization of two novel adenomatous polyposis coli (APC) gene mutations in patients with familial adenomatous polyposis (FAP).
    Bapat B; Berk T; Mitri A; Cohen Z; Gallinger S; Stern H
    Hum Mutat; 1994; 4(4):253-6. PubMed ID: 7866403
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.
    Friedl W; Caspari R; Sengteller M; Uhlhaas S; Lamberti C; Jungck M; Kadmon M; Wolf M; Fahnenstich J; Gebert J; Möslein G; Mangold E; Propping P
    Gut; 2001 Apr; 48(4):515-21. PubMed ID: 11247896
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Incidence and predictive value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients.
    Lam DS; Kwok SP; Kwok AK; Liew CT; Lau JW; Pang CC
    Chin Med J (Engl); 1998 Mar; 111(3):278-81. PubMed ID: 10374435
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital hypertrophy of the retinal pigment epithelium serves as a clinical marker in a family with familial adenomatous polyposis.
    Parisi ML
    J Am Optom Assoc; 1995 Feb; 66(2):106-12. PubMed ID: 7714311
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis.
    Bertario L; Russo A; Sala P; Varesco L; Giarola M; Mondini P; Pierotti M; Spinelli P; Radice P;
    J Clin Oncol; 2003 May; 21(9):1698-707. PubMed ID: 12721244
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotype-genotype correlations in an extended family with adenomatosis coli and an unusual APC gene mutation.
    Ponz de Leon M; Varesco L; Benatti P; Sassatelli R; Izzo P; Scarano MI; Rossi GB; Di Gregorio C; Gismondi V; Percesepe A; de Rosa M; Roncucci L
    Dis Colon Rectum; 2001 Nov; 44(11):1597-604. PubMed ID: 11711730
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancer.
    Chen CS; Phillips KD; Grist S; Bennet G; Craig JE; Muecke JS; Suthers GK
    Fam Cancer; 2006; 5(4):397-404. PubMed ID: 16944273
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Attenuated familial adenomatous polyposis: a case report with mixed features and review of genotype-phenotype correlation.
    Ionescu DN; Papachristou G; Schoen RE; Hedge M; Richards CS; Monzon FA
    Arch Pathol Lab Med; 2005 Nov; 129(11):1401-4. PubMed ID: 16253019
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiplex PCR analysis and genotype-phenotype correlations of frequent APC mutations.
    Cama A; Palmirotta R; Curia MC; Esposito DL; Ranieri A; Ficari F; Valanzano R; Battista P; Modesti A; Tonelli F
    Hum Mutat; 1995; 5(2):144-52. PubMed ID: 7749413
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.