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Journal Abstract Search

97 related items for PubMed ID: 24986476

  • 1. Generalized milia in an infant with full trisomy 13.
    Sugimoto A, Kurokawa T, Kishi K, Yasuda E, Tamai H, Moriwaki S.
    J Dermatol; 2014 Aug; 41(8):763-4. PubMed ID: 24986476
    [No Abstract] [Full Text] [Related]

  • 2. An interesting coexistence of Patau syndrome; Spigelian hernia and undescended testes.
    Demir N, Tuncer O, Peker E, Bilici S, Yavuz A.
    Genet Couns; 2014 Aug; 25(2):241-4. PubMed ID: 25059026
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  • 5. Distal trisomy 10q due to maternal insertional translocation (15;10): A case report and review of literature.
    Türedi Ö, Vícdan A, Yürür Kutlay N.
    Genet Couns; 2016 Aug; 27(2):273-8. PubMed ID: 29485837
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  • 6. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
    Sohn YB, Yun JN, Park SJ, Park MS, Kim SH, Lee JH.
    Ann Clin Lab Sci; 2013 Aug; 43(3):332-6. PubMed ID: 23884231
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  • 9. Chromosome mis-segregation and cytokinesis failure in trisomic human cells.
    Nicholson JM, Macedo JC, Mattingly AJ, Wangsa D, Camps J, Lima V, Gomes AM, Dória S, Ried T, Logarinho E, Cimini D.
    Elife; 2015 May 05; 4():. PubMed ID: 25942454
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  • 10. Engineering of Systematic Elimination of a Targeted Chromosome in Human Cells.
    Sato H, Kato H, Yamaza H, Masuda K, Nguyen HT, Pham TT, Han X, Hirofuji Y, Nonaka K.
    Biomed Res Int; 2017 May 05; 2017():6037159. PubMed ID: 28401157
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  • 14. Autopsy report of a 7-year old patient with the mosaic trisomy 13.
    Imataka G, Yamanouchi H, Hirato J, Eguchi M, Kojima M, Honma K, Arisaka O.
    Cell Biochem Biophys; 2013 Nov 05; 67(2):813-7. PubMed ID: 23526188
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  • 16. Cyclopia, proboscis and alobar holoprosencephaly representative for trisomy 13.
    Bozkurt O, Kanmaz HG, Sahin S, Canpolat FE, Uras N, Oguz SS, Dilmen U.
    Genet Couns; 2014 Nov 05; 25(3):349-51. PubMed ID: 25365860
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  • 17. [Mosaic trisomy 13].
    Cammarata-Scalisi F, Araque D, Lacruz-Rengel MA, Valera-Ruíz B.
    An Pediatr (Barc); 2013 Dec 05; 79(6):402-3. PubMed ID: 23684171
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  • 18. Unusual milia amyloidosis as initial signs of multiple myeloma-associated systemic amyloidosis.
    Ohashi T, Kikuchi N, Yamamoto T.
    Int J Dermatol; 2013 Aug 05; 52(8):981-2. PubMed ID: 23869927
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  • 19. Overlap of Patau and Pierre Robin syndromes along with abnormal metabolism: an interesting case study.
    Jaiswal SK, Sukla KK, Gupta V, Rai AK.
    J Genet; 2014 Dec 05; 93(3):865-8. PubMed ID: 25572249
    [No Abstract] [Full Text] [Related]

  • 20. 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay.
    Rodovalho-Doriqui MJ, Freitas PL, Pinho JD, Cavalli LR, Pereira SR.
    Genet Mol Res; 2013 Jul 24; 12(3):2562-6. PubMed ID: 23979887
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