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PUBMED FOR HANDHELDS

Journal Abstract Search


211 related items for PubMed ID: 34061437

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  • 3. Trisomy 16q21 --> qter: Seven-year follow-up of a girl with unusually long survival.
    de Carvalho AF, da Silva Bellucco FT, dos Santos NP, Pellegrino R, de Azevedo Moreira LM, Toralles MB, Kulikowski LD, Melaragno MI.
    Am J Med Genet A; 2010 Aug; 152A(8):2074-8. PubMed ID: 20635361
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  • 9. Severe upper airway stenosis in a boy with partial monosomy 16p13.3pter and partial trisomy 16q22qter.
    Yamada K, Uchiyama A, Arai M, Kubodera K, Yamamoto Y, Orii KO, Nagasawa H, Masuno M, Kohno Y.
    Congenit Anom (Kyoto); 2009 Jun; 49(2):85-8. PubMed ID: 19489960
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  • 10. A pure de novo 16p13.3 duplication and amplification in a patient with femoral hypoplasia, psychomotor retardation, heart defect, and facial dysmorphism-a case report and literature review of the partial 16p13.3 trisomy syndrome.
    Socha M, Szoszkiewicz A, Simon D, Jamsheer A.
    J Appl Genet; 2023 Feb; 64(1):125-134. PubMed ID: 36586055
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  • 12. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.
    Tos T, Alp MY, Eker HK, Cebi AH, Ikbal M.
    Genet Couns; 2014 Feb; 25(1):35-9. PubMed ID: 24783653
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  • 13. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
    Sohn YB, Yun JN, Park SJ, Park MS, Kim SH, Lee JH.
    Ann Clin Lab Sci; 2013 Feb; 43(3):332-6. PubMed ID: 23884231
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  • 14. Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter.
    Sarri C, Gyftodimou J, Avramopoulos D, Grigoriadou M, Pedersen W, Pandelia E, Pangalos C, Abazis D, Kitsos G, Vassilopoulos D, Brøndum-Nielsen K, Petersen MB.
    Am J Med Genet; 1997 May 02; 70(1):87-94. PubMed ID: 9129747
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  • 15. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
    Schimmenti LA, Higgins RR, Mendelsohn NJ, Casey TM, Steinberger J, Mammel MC, Wiesner GL.
    Am J Med Genet; 1995 May 22; 57(1):52-6. PubMed ID: 7645598
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  • 18. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.
    Quadrelli R, Quadrelli A, Milunsky A, Zou YS, Huang XL, Viera E, Mechoso B, Bellini S, Costabel M, Vaglio A.
    Genet Test Mol Biomarkers; 2009 Jun 22; 13(3):387-93. PubMed ID: 19473082
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  • 20. New findings in partial trisomy 16q: clinical report.
    Sousa B, Rocha G, Doria S, Alves JR, Guedes B, Guimarães H.
    Acta Paediatr; 2004 Jun 22; 93(6):852-4. PubMed ID: 15244241
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