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PUBMED FOR HANDHELDS

Journal Abstract Search


82 related items for PubMed ID: 2741714

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  • 2. Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11).
    Fryns JP, Kleczkowska A.
    Ann Genet; 1987; 30(2):109-10. PubMed ID: 3499841
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  • 3. Ring chromosome 21 and reproductive pattern: a familial case and review of the literature.
    Bertini V, Valetto A, Uccelli A, Tarantino E, Simi P.
    Fertil Steril; 2008 Nov; 90(5):2004.e1-5. PubMed ID: 18371955
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  • 6. Ring chromosome 21 in a normal female.
    Kleczkowska A, Fryns JP.
    Ann Genet; 1984 Nov; 27(2):126-8. PubMed ID: 6331791
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  • 7. [Prenatal diagnosis of 3 cases of ring G chromosomes: one 21 and two 22, one of which was de novo].
    Crusi A, Engel E.
    Ann Genet; 1986 Nov; 29(4):253-60. PubMed ID: 3495227
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  • 8. Acute lymphoblastic leukemia in a child with constitutional ring chromosome 21.
    Falchi AM, Orofino MG, Nucaro AL, De Virgiliis S, Cao A.
    Cancer Genet Cytogenet; 1987 Aug; 27(2):219-24. PubMed ID: 3474055
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  • 9. [Cytogenetic analysis and phenotype location analysis on the karyotype of a ring chromosome 21 syndrome].
    Zhu XY, Zhao R, Ye ZC, Peng YG, Tan YQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):682-3. PubMed ID: 16331572
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  • 13. Complete karyotype discrepancy between placental and fetal cells in a case of ring chromosome 18.
    Fischer W, Dermitzel A, Osmers R, Pruggmayer M.
    Prenat Diagn; 2001 Jun; 21(6):481-3. PubMed ID: 11438954
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  • 14. Characterization of a small supernumerary marker chromosome as r(8) at prenatal diagnosis by MFISH.
    Gole LA, Biswas A.
    Prenat Diagn; 2005 Jan; 25(1):73-8. PubMed ID: 15662692
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  • 16. Ocular findings in a patient with deletion short arm chromosome 5 (cri du chat) and ring chromosome 14.
    Clark DI, Howard PJ, Patterson A.
    Trans Ophthalmol Soc U K (1962); 1986 Jan; 105 ( Pt 6)():723-5. PubMed ID: 3477901
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  • 17. Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.
    Knegt AC, Li S, Engelen JJ, Bijlsma EK, Warburton PE.
    Prenat Diagn; 2003 Mar; 23(3):215-20. PubMed ID: 12627422
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  • 18. Familial ring (19) chromosome mosaicism: case report and review.
    Flejter WL, Finlinson D, Root S, Nguyen W, Brothman AR, Viskochil D.
    Am J Med Genet; 1996 Dec 18; 66(3):276-80. PubMed ID: 8985487
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  • 20. [A case of a girl with a ring chromosome 18 in the karyotype].
    Midro AT, Czerwińska-Ciechan K, Wiśniewski L, Sawicka A, Marcinkiewicz D.
    Pol Tyg Lek; 1987 Mar 02; 42(9):260-3. PubMed ID: 3601789
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