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PUBMED FOR HANDHELDS

Journal Abstract Search

239 related items for PubMed ID: 8042676

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  • 7. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS, Gibson L, McGrath J, Meyn MS, Breg WR, Yang-Feng TL.
    Am J Med Genet; 1993 May 15; 46(3):288-92. PubMed ID: 8488873
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  • 12. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
    Mewar R, Harrison W, Weaver DD, Palmer C, Davee MA, Overhauser J.
    Am J Med Genet; 1994 Aug 15; 52(2):178-83. PubMed ID: 7802005
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  • 13. Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:).
    Fryns JP, Kleczkowska A, Vogels A, Van den Berghe H.
    Ann Genet; 1989 Aug 15; 32(3):171-3. PubMed ID: 2573313
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  • 15. U-type exchange in a paracentric inversion as a possible mechanism of origin of an inverted tandem duplication of chromosome 8.
    Mitchell JJ, Vekemans M, Luscombe S, Hayden M, Weber B, Richter A, Sparkes R, Kojis T, Watters G, Der Kaloustian VM.
    Am J Med Genet; 1994 Feb 15; 49(4):384-7. PubMed ID: 8160729
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  • 18. Isochromosome-formation in chromosome 9.
    Miller K, Arslan-Kirchner M.
    Ann Genet; 1994 Feb 15; 37(2):78-81. PubMed ID: 7985983
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  • 19. De novo inverted tandem duplication of the long arm of chromosome 2(q34 leads to q37).
    Yu CW, Chen H.
    Birth Defects Orig Artic Ser; 1982 Feb 15; 18(3B):311-20. PubMed ID: 7139114
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  • 20. Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.
    Sireteanu A, Braha E, Popescu R, Gramescu M, Gorduza EV, Rusu C.
    Rev Med Chir Soc Med Nat Iasi; 2013 Feb 15; 117(3):731-4. PubMed ID: 24502041
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