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Journal Abstract Search

546 related items for PubMed ID: 25365851

  • 1. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
    Brambila-Tapia AJ, Neira VA, Vásquez-Velásquez AI, Jimenez-Arredondo RE, Chávez-González EL, Picos-Cárdenas VJ, Fletes-Rayas AL, Figuera LE.
    Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
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  • 2. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
    Akbas E, Polat S, Karakas-Celik S, Altintas ZM, Yildirim M, Yilgor E.
    Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
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  • 3. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
    Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP.
    Genet Couns; 1998; 9(3):215-21. PubMed ID: 9777345
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  • 4. 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; 19(4):365-71. PubMed ID: 19239079
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  • 5. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
    Mutesa L, Hellin AC, Jamar M, Pierquin G, Bours V, Verloes A.
    Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
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  • 6. A unique combination of 17pter trisomy and 21qter monosomy in a boy with developmental delay, severe intellectual disability, growth retardation and dysmorphisms.
    Zheng Z, Yao RE, Geng J, Jin X, Shen Y, Ying D, Fu Q, Yu Y.
    Gene; 2013 Mar 10; 516(2):301-6. PubMed ID: 23296059
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  • 10. A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature.
    Paththinige CS, Sirisena ND, Kariyawasam UGIU, Ediriweera RC, Kruszka P, Muenke M, Dissanayake VHW.
    BMC Med Genomics; 2018 May 08; 11(1):44. PubMed ID: 29739404
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  • 12. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
    Courtens W, Wauters J, Wojciechowski M, Reyniers E, Scheers S, van Luijk R, Rooms L, Kooy F, Wuyts W.
    Clin Dysmorphol; 2007 Oct 08; 16(4):231-9. PubMed ID: 17786114
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  • 13. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
    Recalcati MP, Bellini M, Norsa L, Ballarati L, Caselli R, Russo S, Larizza L, Giardino D.
    Gene; 2012 Jul 01; 502(1):40-5. PubMed ID: 22537675
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  • 15. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA, Kamel AK, Ismail S, Helmy NA, Aglan MS, El Gammal M, El Ruby M, Mohamed AM.
    Genet Couns; 2007 Jul 01; 18(1):29-48. PubMed ID: 17515299
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  • 16. Partial trisomy 17q and monosomy 9p due to a familial translocation.
    Cotter PD, Stewart NL.
    Ann Genet; 1990 Jul 01; 33(4):231-3. PubMed ID: 1710432
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  • 17. Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q.
    Martín-De Saro MD, Valdés-Miranda JM, Plaza-Benhumea L, Pérez-Cabrera A, Gonzalez-Huerta LM, Guevara-Yañez R, Cuevas-Covarrubias SA.
    Cytogenet Genome Res; 2015 Jul 01; 147(2-3):124-9. PubMed ID: 26900692
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  • 18. Unusual Chromosomal Rearrangement Resulted in Interstitial Monosomy 9p: Case Report.
    Durmaz CD, Yararbaş K, Kutlay NY, Türedi Ö, Akın İ, Gürbüz C, Karataş G, Tükün A.
    Cytogenet Genome Res; 2016 Jul 01; 148(1):19-24. PubMed ID: 27166162
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