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PUBMED FOR HANDHELDS

Journal Abstract Search


175 related items for PubMed ID: 18568304

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  • 3. Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays.
    Lyons MJ, Fuller JD, Montoya Mdel C, DuPont BR, Holden KR.
    J Child Neurol; 2013 Apr; 28(4):524-6. PubMed ID: 22752474
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  • 4. Trisomy 7p resulting from 7p15;9p24 translocation: report of a new case and review of associated medical complications.
    Kozma C, Haddad BR, Meck JM.
    Am J Med Genet; 2000 Apr 10; 91(4):286-90. PubMed ID: 10766985
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  • 5. 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 Apr 10; 25(1):35-9. PubMed ID: 24783653
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  • 7. Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation.
    Frints SG, Moerman P, Fryns JP.
    Genet Couns; 1996 Apr 10; 7(4):313-9. PubMed ID: 8985736
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  • 8. Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature.
    Schmidt B, Udink ten Cate F, Weiss M, Koehler U.
    Eur J Pediatr; 2012 Jul 10; 171(7):1047-53. PubMed ID: 22302461
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  • 10. 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 Jul 10; 7(1):61-5. PubMed ID: 8652090
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  • 11. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Huang JK, Lee CC, Wang W.
    Genet Couns; 2006 Jul 10; 17(1):57-63. PubMed ID: 16719278
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  • 14. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Chern SR, Lee CC, Chen YJ, Wang W.
    Prenat Diagn; 2005 Dec 10; 25(12):1170-2. PubMed ID: 16315335
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  • 16. 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 Dec 10; 25(3):289-97. PubMed ID: 25365851
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  • 20. 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 10; 13(3):387-93. PubMed ID: 19473082
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