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Journal Abstract Search

37 related items for PubMed ID: 9852686

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  • 3. Two polymorphic AvaI and HhaI sites in a differentially methylated region of the human H19 gene.
    Miyatake S, Ikeda Y, Jinno Y, Niikawa N.
    Jpn J Hum Genet; 1996 Jun; 41(2):253-5. PubMed ID: 8771991
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  • 4. Lack of imprinting of the human dopamine D4 receptor (DRD4) gene.
    Cichon S, Nöthen MM, Wolf HK, Propping P.
    Am J Med Genet; 1996 Apr 09; 67(2):229-31. PubMed ID: 8723054
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  • 5. Parentally imprinted allele (PIA) typing in the differentially methylated region upstream of the human H19 gene.
    Huang D, Lin X, Chen H, Yang Q, Jie Y, Zhai X, Yin H.
    Forensic Sci Int Genet; 2008 Sep 09; 2(4):286-91. PubMed ID: 19083838
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  • 6. Frequency and timing of loss of imprinting at 11p13 and 11p15 in Wilms' tumor development.
    Brown KW, Power F, Moore B, Charles AK, Malik KT.
    Mol Cancer Res; 2008 Jul 09; 6(7):1114-23. PubMed ID: 18644976
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  • 7. Loss of imprinting and genetic alterations of the cyclin-dependent kinase inhibitor p57KIP2 gene in head and neck squamous cell carcinoma.
    Lai S, Goepfert H, Gillenwater AM, Luna MA, El-Naggar AK.
    Clin Cancer Res; 2000 Aug 09; 6(8):3172-6. PubMed ID: 10955800
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  • 8. Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5.
    Bajaj V, Markandaya M, Krishna L, Kumar A.
    BMC Genet; 2004 Jun 03; 5():13. PubMed ID: 15175115
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  • 9. Epigenetic deregulation of imprinting in congenital diseases of aberrant growth.
    Delaval K, Wagschal A, Feil R.
    Bioessays; 2006 May 03; 28(5):453-9. PubMed ID: 16615080
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  • 10. A SacII polymorphism in the human ASCL2 (HASH2) gene region.
    Miyamoto T, Jinno Y, Miura K, Sengoku K, Soejima H, Yun K, Yaginuma Y, Niikawa N, Ishikawa M.
    J Hum Genet; 1998 May 03; 43(1):69-70. PubMed ID: 9610003
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  • 11. Methylation status of putative differentially methylated regions of porcine IGF2 and H19.
    Han DW, Im YB, Do JT, Gupta MK, Uhm SJ, Kim JH, Schöler HR, Lee HT.
    Mol Reprod Dev; 2008 May 03; 75(5):777-84. PubMed ID: 18247333
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  • 15. Novel splicing of an IGF2 polymorphic region in human adrenocortical carcinomas.
    Gray SG, Kjellman M, Larsson C, Ekström TJ.
    Biochem Biophys Res Commun; 1997 Oct 29; 239(3):878-83. PubMed ID: 9367863
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  • 17. Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting.
    Lee MP, Brandenburg S, Landes GM, Adams M, Miller G, Feinberg AP.
    Hum Mol Genet; 1999 Apr 29; 8(4):683-90. PubMed ID: 10072438
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  • 18. [Screening for imprinted genes by allelic message display].
    Hagiwara Y, Ito T.
    Tanpakushitsu Kakusan Koso; 1997 Dec 29; 42(17 Suppl):2864-8. PubMed ID: 9455205
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  • 19. A frequent polymorphism in the 5' region of the BCMA gene.
    Roetto A, Cicilano M, Gottardi E, Totaro A, Carella M, Gasparini P, Camaschella C.
    Mol Cell Probes; 1997 Aug 29; 11(4):311-2. PubMed ID: 9281419
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  • 20. Human polymorphic probe pE1.8 detects SacI polymorphism in the ribonucleotide reductase M1 subunit gene.
    Byrne J, Smith P.
    Hum Genet; 1991 Jul 29; 87(3):376. PubMed ID: 1677928
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