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Journal Abstract Search

160 related items for PubMed ID: 2288464

  • 1. [Proximal monosomy 13].
    Geormăneanu M, Geormăneanu C.
    Ann Genet; 1990; 33(3):176-8. PubMed ID: 2288464
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  • 2. Duplication 16q12----qter arising from 3:1 segregation in a 46,XX,t(13;16) (q12;q12) mother.
    Pérez-Castillo A, Martin-Lucas MA, Abrisqueta JA.
    Ann Genet; 1990; 33(2):121-3. PubMed ID: 2241087
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  • 3. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP, Kleczkowska A, Jaeken J, Van Herck K, Van den Berghe MH.
    Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064
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  • 4. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J, Chernos J, Roland B.
    Am J Med Genet; 1997 Dec 19; 73(3):327-9. PubMed ID: 9415693
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  • 6. Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family.
    Wilroy RS, Summitt RL, Martens P, Gooch WM.
    Ann Genet; 1977 Dec 19; 20(4):237-42. PubMed ID: 305749
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  • 8. Distal monosomy of the long arm of chromosome 6 (6q25----6qter) inherited by maternal translocation t(6q;17q).
    Oliveira-Duarte MH, Martelli-Soares LR, Sarquis-Cintra T, Machado ML, Lison MP.
    Ann Genet; 1990 Dec 19; 33(1):56-9. PubMed ID: 2195984
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  • 9. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat].
    Di Cesare D, Paludetto R, Casullo C, Pagano L, Stabile M, Sicolo A, Ventruto V.
    Minerva Pediatr; 1980 Dec 15; 32(23):1349-52. PubMed ID: 7219376
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  • 10. Partial 4q duplication due to inherited der(20), t(4;20)(q25;q13)mat.
    Sparkes RS, Francke U, Muller H, Toomey K.
    Ann Genet; 1977 Mar 15; 20(1):31-5. PubMed ID: 302670
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  • 11. De novo partial monosomy 21 with unusual karyotype.
    Al-Awadi SA, Naguib KK, Teebi AS, Sundareshan TS.
    Jinrui Idengaku Zasshi; 1986 Mar 15; 31(1):45-8. PubMed ID: 3735757
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  • 15. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
    Ausems MG, Van Spijker HG, Dijkhuis HJ, Swanenburg De Veye HF, Bijlsma JB.
    Genet Couns; 1996 Mar 15; 7(1):61-5. PubMed ID: 8652090
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  • 16. A case of partial 9p monosomy with some unusual clinical features.
    Rutten FJ, Hustinx TW, Dunk-Tillemans AA, Scheres JM, Tjon YS.
    Ann Genet; 1978 Mar 15; 21(1):51-5. PubMed ID: 308344
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  • 20. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
    Qumsiyeh MB, Stevens CA.
    Am J Med Genet; 1993 Sep 01; 47(3):387-91. PubMed ID: 8135287
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