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Journal Abstract Search

119 related items for PubMed ID: 11354413

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  • 3. Molecular abnormalities in pediatric embryonal brain tumors--analysis of loss of heterozygosity on chromosomes 1, 5, 9, 10, 11, 16, 17 and 22.
    Zakrzewska M, Rieske P, Debiec-Rychter M, Zakrzewski K, Polis L, Fiks T, Liberski PP.
    Clin Neuropathol; 2004; 23(5):209-17. PubMed ID: 15581023
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  • 4. Molecular genetic studies of chromosome 11 and chromosome 22q DNA sequences in pediatric medulloblastomas.
    Lescop S, Lellouch-Tubiana A, Vassal G, Besnard-Guerin C.
    J Neurooncol; 1999 Sep; 44(2):119-27. PubMed ID: 10619495
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  • 5. Loss of heterozygosity on chromosome 10q associated with malignancy and prognosis in astrocytic tumors, and discovery of novel loss regions.
    Daido S, Takao S, Tamiya T, Ono Y, Terada K, Ito S, Ouchida M, Date I, Ohmoto T, Shimizu K.
    Oncol Rep; 2004 Oct; 12(4):789-95. PubMed ID: 15375501
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  • 6. Molecular genetic studies in medulloblastomas: evidence for tumor suppressor genes at the chromosomal regions 1q31-32 and 17p13.
    Pietsch T, Koch A, Wiestler OD.
    Klin Padiatr; 1997 Oct; 209(4):150-5. PubMed ID: 9293446
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  • 10. Comprehensive loss of heterozygosity analysis and identification of a novel hotspot at 3p21 in salivary gland neoplasms.
    Honjo N, Gunduz M, Fukushima K, Cengiz B, Beder LB, Gunduz E, Nagatsuka H, Xiao J, Shimizu K, Nishizaki K.
    Otolaryngol Head Neck Surg; 2007 Jul; 137(1):119-25. PubMed ID: 17599578
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  • 11. Allelic loss and replication errors at microsatellite loci on chromosome 11p in head and neck squamous carcinoma: association with aggressive biological features.
    El-Naggar AK, Hurr K, Huff V, Luna MA, Goepfert H, Batsakis JG.
    Clin Cancer Res; 1996 May; 2(5):903-7. PubMed ID: 9816248
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  • 12. Genetic aberration on chromosome 10 in human oral squamous cell carcinoma.
    Yamashita Y, Miyakawa A, Mochida Y, Aisaki K, Yama M, Shiiba M, Watanabe T, Yokoe H, Uzawa K, Imai Y, Tanzawa H.
    Int J Oncol; 2002 Mar; 20(3):595-8. PubMed ID: 11836574
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  • 14. Loss of heterozygosity in the MXI1 gene is a frequent occurrence in melanoma.
    Ariyanayagam-Baksh SM, Baksh FK, Swalsky PA, Finkelstein SD.
    Mod Pathol; 2003 Oct; 16(10):992-5. PubMed ID: 14559981
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  • 16. Allelic loss of chromosomes 16q and 10q in human prostate cancer.
    Carter BS, Ewing CM, Ward WS, Treiger BF, Aalders TW, Schalken JA, Epstein JI, Isaacs WB.
    Proc Natl Acad Sci U S A; 1990 Nov; 87(22):8751-5. PubMed ID: 1978938
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  • 17. [Genome-wide genetic study of medulloblastoma using allelotype analysis].
    Yin XL, Pang CS, Ng HK.
    Zhonghua Bing Li Xue Za Zhi; 2004 Oct; 33(5):413-5. PubMed ID: 15498208
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