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Pubmed for Handhelds

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Journal Abstract Search

77 related items for PubMed ID: 3866853

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  • 10. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
    García-Cruz D, García-Esquivel L, Rivera H, Vaca G, Rolón A, Cantú JM.
    Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157
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  • 11. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
    Cora T, Acar H, Oran B.
    Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
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  • 12. [Partial 13 trisomy by maternal 46, XX, t (3; 13) (p 26; q 21) translocation].
    Stoll C, Halb A.
    Pediatrie; 1974; 29(7):725-9. PubMed ID: 4456285
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  • 13. Unusual 13/13 translocation and 13 trisomy phenotype.
    Fryns JP, Kleczkowska A, Kubien E.
    Ann Genet; 1982; 25(2):113-5. PubMed ID: 6984626
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  • 16. Partial trisomy 13 with phenotype of Patau syndrome due to maternal reciprocal translocation t(6;13) (q25;q13).
    Petit P, Fryns JP, van den Berghe H.
    Ann Genet; 1980; 23(1):57-9. PubMed ID: 6965845
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  • 17. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA, Mikel'saar AV, Mikel'saar RV.
    Sov Genet; 1974 Jun 01; 8(5):651-7. PubMed ID: 4413436
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  • 20. [Partial trisomy C by t(Cq-; Dp+) translocation with a C(p- q+) remnant].
    De Grouchy J, Thieffry S, Aicardi J, Chevrie JJ, Zucker G.
    Arch Fr Pediatr; 1967 Oct 01; 24(8):859-68. PubMed ID: 5584189
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