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Journal Abstract Search

152 related items for PubMed ID: 3258493

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  • 3. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
    Battaglia A, Brothman AR, Carey JC.
    Am J Med Genet; 2002 Sep 15; 112(1):103-6. PubMed ID: 12239731
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  • 5. 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 Sep 15; 48(3):355-9. PubMed ID: 16179232
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  • 6. Familial 10p trisomy resulting from a maternal pericentric inversion.
    Kozma C, Meck JM.
    Am J Med Genet; 1994 Feb 01; 49(3):281-7. PubMed ID: 8209887
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  • 11. Natural history of mosaic trisomy 14 syndrome.
    Fujimoto A, Allanson J, Crowe CA, Lipson MH, Johnson VP.
    Am J Med Genet; 1992 Sep 15; 44(2):189-96. PubMed ID: 1456290
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  • 12. Sensorineural deafness in two infants: a novel feature in the 22q distal duplication syndrome. Cardinal signs in trisomies 22 subtypes.
    Barajas-Barajas LO, Valdez LL, Gonzalez JR, García-García C, Rivera H, Ramírez L.
    Genet Couns; 2004 Sep 15; 15(2):167-73. PubMed ID: 15287416
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  • 17. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H, Vermeesch J, Fryns JP.
    Genet Couns; 2008 Sep 15; 19(4):365-71. PubMed ID: 19239079
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  • 18. Trisomy 14 mosaicism in a 5-year-old boy.
    Vachvanichsanong P, Jinorose U, Sangnuachua P.
    Am J Med Genet; 1991 Jul 01; 40(1):80-3. PubMed ID: 1887854
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  • 20. The phenotypic and cytogenetic spectrum of partial trisomy 9.
    Wilson GN, Raj A, Baker D.
    Am J Med Genet; 1985 Feb 01; 20(2):277-82. PubMed ID: 3976721
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