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Journal Abstract Search

340 related items for PubMed ID: 15996211

  • 1. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
    Mark HF, Wyandt H, Huang XL, Milunsky JM.
    Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
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  • 3. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
    Bartsch O, Rasi S, Hoffmann K, Blin N.
    Eur J Hum Genet; 2005 May; 13(5):592-8. PubMed ID: 15756300
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  • 4. [Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].
    Stankiewicz P, Korniszewski L, Bocian E, Stańczak H.
    Pediatr Pol; 1996 Mar; 71(3):241-5. PubMed ID: 8966096
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  • 7. Cytogenetic characterization of cat eye syndrome marker chromosome.
    Wenger SL, Surti U, Nwokoro NA, Steele MW.
    Ann Genet; 1994 Mar; 37(1):33-6. PubMed ID: 8010712
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  • 8. Trisomy 22 confirmed by fluorescent in situ hybridization.
    Stratton RF, DuPont BR, Mattern VL, Young RS, McCourt JW, Moore CM.
    Am J Med Genet; 1993 Apr 01; 46(1):109-12. PubMed ID: 8494030
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  • 10. Costovertebral dysplasia in a patient with partial trisomy 22.
    Tonk V, Wilson G, Schutt R, Mock J, Wyandt H, Mark HF, Ito M.
    Exp Mol Pathol; 2006 Apr 01; 80(2):197-200. PubMed ID: 16259976
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  • 11. Prenatal diagnosis of partial trisomy through in situ hybridization on amniocytes with whole chromosome and centromere-specific DNA probes. A case report.
    Blancato JK, Eglinton G, George J, Benkendorf J, Pinckert T, Meck J.
    J Reprod Med; 1995 Jul 01; 40(7):537-9. PubMed ID: 7473445
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  • 15. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
    Huang XL, de Michelena MI, Mark H, Harston R, Benke PJ, Price SJ, Milunsky A.
    Clin Genet; 2005 Dec 01; 68(6):513-9. PubMed ID: 16283881
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  • 16. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM.
    Am J Med Genet; 1994 Mar 01; 50(1):21-7. PubMed ID: 8160748
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  • 18. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
    de Ravel T, Aerssens P, Vermeesch JR, Fryns JP.
    Eur J Med Genet; 2005 Mar 01; 48(3):355-9. PubMed ID: 16179232
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  • 20. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
    Rao VV, Carpenter NJ, Gucsavas M, Coldwell J, Say B.
    Am J Med Genet; 1995 Jul 31; 58(1):50-3. PubMed ID: 7573156
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