BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 7953248)

  • 1. Diagnosis of retinoblastoma in a presymptomatic stage after detection of interstitial chromosomal deletion 13q.
    Kennerknecht I; Barbi G; Greher J
    Ophthalmic Genet; 1994 Mar; 15(1):19-24. PubMed ID: 7953248
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lymphocyte chromosome survey in 42 patients with retinoblastoma: effort to detect 13q14 deletion mosaicism.
    Motegi T
    Hum Genet; 1981; 58(2):168-73. PubMed ID: 7287000
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A genetic study of retinoblastoma.
    Liu XX; Sun YJ; Zhang L
    J Tongji Med Univ; 1991; 11(4):220-4. PubMed ID: 1819032
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sporadic bilateral retinoblastoma and 13q- chromosomal deletion.
    Francke U; Kung F
    Med Pediatr Oncol; 1976; 2(4):379-85. PubMed ID: 1004381
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A case report of a patient with retinoblastoma and chromosome 13q deletion: assignment of a new gene (gene for LCP1) on human chromosome 13.
    Kondo I; Shin K; Honmura S; Nakajima H; Yamamura E; Satoh H; Terauchi M; Usuki Y; Takita H; Hamaguchi H
    Hum Genet; 1985; 71(3):263-6. PubMed ID: 3864729
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Early diagnosis of retinoblastoma based on dysmorphic features and karyotype analysis.
    Seidman DJ; Shields JA; Augsburger JJ; Nelson LB; Lee ML; Sciorra LJ
    Ophthalmology; 1987 Jun; 94(6):663-6. PubMed ID: 3627714
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Constitutional karyotype in retinoblastoma. Case report and review of literature.
    Munier F; Pescia G; Jotterand-Bellomo M; Balmer A; Gailloud C; Thonney F
    Ophthalmic Paediatr Genet; 1989 Jun; 10(2):129-50. PubMed ID: 2674826
    [TBL] [Abstract][Full Text] [Related]  

  • 8. First cytogenetic evidence of homozygosity for the retinoblastoma deletion in chromosome 13.
    Lemieux N; Milot J; Barsoum-Homsy M; Michaud J; Leung TK; Richer CL
    Cancer Genet Cytogenet; 1989 Nov; 43(1):73-8. PubMed ID: 2790775
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial retinoblastoma (mother and son) with 13q14 deletion.
    Fukushima Y; Kuroki Y; Ito T; Kondo I; Nishigaki I
    Hum Genet; 1987 Oct; 77(2):104-7. PubMed ID: 3653883
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion of 13q in two patients with retinoblastoma, one probably due to 13q-mosaicism in the mother.
    Michalová K; Kloucek F; Musilová J
    Hum Genet; 1982; 61(3):264-6. PubMed ID: 7173873
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytogenetic evidence of multifocal origin of a unilateral retinoblastoma. A help in genetic counseling.
    Tien HF; Chuang SM; Chen MS; Lee FY; Hou PK
    Cancer Genet Cytogenet; 1989 Oct; 42(2):203-8. PubMed ID: 2790755
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Interstitial deletion of 13q and a 13;X chromosome translocation results in partial trisomy 13 and bilateral retinoblastoma.
    Dries D; Baca K; Truss L; Dobin S
    Ophthalmic Genet; 2003 Sep; 24(3):175-80. PubMed ID: 12868036
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deletion (13)(q13q14.3) with retinoblastoma: confirmation and extension of a recognisable pattern of clinical features in retinoblastoma patients with 13q deletion.
    Motegi T; Ikeda K; Watanabe K; Yanagawa Y; Minoda K
    J Med Genet; 1987 Nov; 24(11):696-7. PubMed ID: 3430545
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequency of 13q abnormalities among 203 patients with retinoblastoma.
    Bunin GR; Emanuel BS; Meadows AT; Buckley JD; Woods WG; Hammond GD
    J Natl Cancer Inst; 1989 Mar; 81(5):370-4. PubMed ID: 2915374
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A chromosomal breakpoint that separates the esterase D and retinoblastoma predisposition loci in a patient with del(13)(q14q31).
    Cowell JK; Hungerford J; Rutland P; Jay M
    Cancer Genet Cytogenet; 1987 Jul; 27(1):27-31. PubMed ID: 3472646
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Failure to thrive leading to early detection of retinoblastoma.
    Kingston JE; Clark J; Santos H; Jones D; Hungerford JL
    Pediatr Hematol Oncol; 1990; 7(2):199-203. PubMed ID: 2206862
    [No Abstract]   [Full Text] [Related]  

  • 17. Bilateral retinoblastoma associated with 13q-mosaicism. Possible manifestation of a germinal mutation.
    Ribeiro MC; Andrade JA; Erwenne CM; Brunoni D
    Cancer Genet Cytogenet; 1988 Jun; 32(2):169-75. PubMed ID: 3365680
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lymphocyte chromosome survey in 80 patients with retinoblastoma.
    Mao WS; Lin XH; Ma QY; Chen YZ; Zeng LH; Dai ZY
    Yan Ke Xue Bao; 1989 Jun; 5(1-2):7-13. PubMed ID: 2485748
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Retinoblastoma and interstitial deletion of 13q (author's transl)].
    De Grouchy J; Turleau C; Cabanis MO; Richardet JM
    Arch Fr Pediatr; 1980 Oct; 37(8):531-5. PubMed ID: 7447607
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Retinoblastoma and subband deletion of chromosome 13.
    Yunis JJ; Ramsay N
    Am J Dis Child; 1978 Feb; 132(2):161-3. PubMed ID: 626181
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.