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Journal Abstract Search

488 related items for PubMed ID: 21145667

  • 1. De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features.
    Debost-Legrand A, Capri Y, Gouas L, Pebrel-Richard C, Veronese L, Tchirkov A, Haoud K, Boespflug-Tanguy O, Goumy C, Vago P.
    Pathol Biol (Paris); 2011 Dec; 59(6):309-13. PubMed ID: 21145667
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  • 6. Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotype.
    Giannikou K, Fryssira H, Oikonomakis V, Syrmou A, Kosma K, Tzetis M, Kitsiou-Tzeli S, Kanavakis E.
    Gene; 2012 Sep 15; 506(2):360-8. PubMed ID: 22766398
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  • 10. A de novo complex chromosomal rearrangement involving chromosomes 2, 8 and 13 in a dysmorphic case with polysyndactyly.
    Karaman B, Rosti RO, Yilmaz K, Oztürk H, Kayserili H, Başaran S.
    Turk J Pediatr; 2009 Sep 15; 51(6):613-6. PubMed ID: 20196399
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  • 11. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
    Simovich MJ, Yatsenko SA, Kang SH, Cheung SW, Dudek ME, Pursley A, Ward PA, Patel A, Lupski JR.
    Prenat Diagn; 2007 Dec 15; 27(12):1112-7. PubMed ID: 17849500
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  • 12. [Array comparative genomic hybridization detection of a de novo 4q21.21-q22.1 deletion in a child with severe growth retardation].
    Zhou J, Hu P, Liu A, Li L, Ji X, Hui W, Wang Y, Xu Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb 15; 31(1):52-5. PubMed ID: 24510563
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  • 13. Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
    Davidsson J, Collin A, Björkhem G, Soller M.
    BMC Med Genet; 2008 Jan 14; 9():2. PubMed ID: 18194513
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  • 14. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
    Xiao B, Ji X, Jiang WT, Zhang JM, Hu Q, Tao J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec 14; 28(6):654-7. PubMed ID: 22161098
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  • 18. The usefulness of array comparative genomic hybridization in clinical diagnostics of intellectual disability in children.
    Bartnik M, Wiśniowiecka-Kowalnik B, Nowakowska B, Smyk M, Kędzior M, Sobecka K, Kutkowska-Kaźmierczak A, Klapecki J, Szczałuba K, Castañeda J, Własienko P, Bezniakow N, Obersztyn E, Bocian E.
    Dev Period Med; 2014 Dec 14; 18(3):307-17. PubMed ID: 25182394
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  • 19. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
    Schluth-Bolard C, Delobel B, Sanlaville D, Boute O, Cuisset JM, Sukno S, Labalme A, Duban-Bedu B, Plessis G, Jaillard S, Dubourg C, Henry C, Lucas J, Odent S, Pasquier L, Copin H, Latour P, Cordier MP, Nadeau G, Till M, Edery P, Andrieux J.
    Eur J Med Genet; 2009 Dec 14; 52(5):291-6. PubMed ID: 19505601
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  • 20. Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation.
    Palka-Bayard-de-Volo C, De Marco S, Chiavaroli V, Alfonsi M, Calabrese G, Chiarelli F, Mohn A.
    Gene; 2012 Aug 01; 504(1):107-10. PubMed ID: 22583828
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