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Journal Abstract Search

726 related items for PubMed ID: 25539807

  • 1. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
    D'Amours G, Langlois M, Mathonnet G, Fetni R, Nizard S, Srour M, Tihy F, Phillips MS, Michaud JL, Lemyre E.
    BMC Med Genomics; 2014 Dec 24; 7():70. PubMed ID: 25539807
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  • 2. Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation.
    Tucker T, Montpetit A, Chai D, Chan S, Chénier S, Coe BP, Delaney A, Eydoux P, Lam WL, Langlois S, Lemyre E, Marra M, Qian H, Rouleau GA, Vincent D, Michaud JL, Friedman JM.
    BMC Med Genomics; 2011 Mar 25; 4():25. PubMed ID: 21439053
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  • 3. Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
    Shoukier M, Klein N, Auber B, Wickert J, Schröder J, Zoll B, Burfeind P, Bartels I, Alsat EA, Lingen M, Grzmil P, Schulze S, Keyser J, Weise D, Borchers M, Hobbiebrunken E, Röbl M, Gärtner J, Brockmann K, Zirn B.
    Clin Genet; 2013 Jan 25; 83(1):53-65. PubMed ID: 22283495
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  • 4. 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 Jan 25; 18(3):307-17. PubMed ID: 25182394
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  • 5. Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping.
    Bruno DL, White SM, Ganesamoorthy D, Burgess T, Butler K, Corrie S, Francis D, Hills L, Prabhakara K, Ngo C, Norris F, Oertel R, Pertile MD, Stark Z, Amor DJ, Slater HR.
    J Med Genet; 2011 Dec 25; 48(12):831-9. PubMed ID: 22039585
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  • 6. High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical setting.
    Wincent J, Anderlid BM, Lagerberg M, Nordenskjöld M, Schoumans J.
    Clin Genet; 2011 Feb 25; 79(2):147-57. PubMed ID: 20486943
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  • 7. The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.
    Wayhelova M, Smetana J, Vallova V, Hladilkova E, Filkova H, Hanakova M, Vilemova M, Nikolova P, Gromesova B, Gaillyova R, Kuglik P.
    BMC Med Genomics; 2019 Jul 23; 12(1):111. PubMed ID: 31337399
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  • 14. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
    Cappuccio G, Vitiello F, Casertano A, Fontana P, Genesio R, Bruzzese D, Ginocchio VM, Mormile A, Nitsch L, Andria G, Melis D.
    Ital J Pediatr; 2016 Apr 12; 42():39. PubMed ID: 27072107
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  • 17. [Molecular diagnosis of children with unexplained intellectual disability/ developmental delay by array-CGH].
    He XY, Chen XC, Li R, Li P, Lu AM.
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 May 12; 17(5):459-63. PubMed ID: 26014695
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  • 18. Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalities.
    Mason-Suares H, Kim W, Grimmett L, Williams ES, Horner VL, Kunig D, Goldlust IS, Wu BL, Shen Y, Miller DT, Martin CL, Rudd MK.
    Genet Med; 2013 Sep 12; 15(9):706-12. PubMed ID: 23558256
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  • 19. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
    Kloth JN, Oosting J, van Wezel T, Szuhai K, Knijnenburg J, Gorter A, Kenter GG, Fleuren GJ, Jordanova ES.
    BMC Genomics; 2007 Feb 20; 8():53. PubMed ID: 17311676
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