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Journal Abstract Search

229 related items for PubMed ID: 15793836

  • 1. A girl with inverted triplication of chromosome 3q25.3 --> q29 and multiple congenital anomalies consistent with 3q duplication syndrome.
    Ounap K, Ilus T, Bartsch O.
    Am J Med Genet A; 2005 May 01; 134(4):434-8. PubMed ID: 15793836
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  • 2. Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24-q26.31 with minimal overlap to the dup(3q) critical region.
    Meins M, Hagh JK, Gerresheim F, Einhoff E, Olschewski H, Strehl H, Epplen JT.
    Am J Med Genet A; 2005 Jan 01; 132A(1):84-9. PubMed ID: 15551338
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  • 3. Further delineation of the dup(3q) syndrome.
    Wilson GN, Dasouki M, Barr M.
    Am J Med Genet; 1985 Sep 01; 22(1):117-23. PubMed ID: 4050847
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  • 4. Partial duplication of 3q (q25.1-->q26.1) without the Brachmann-de Lange phenotype.
    Lopez-Rangel E, Dill FJ, Hrynchak MA, Van Allen MI.
    Am J Med Genet; 1993 Nov 15; 47(7):1068-71. PubMed ID: 8291525
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  • 5. Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).
    Allderdice PW, Browne N, Murphy DP.
    Am J Hum Genet; 1975 Nov 15; 27(6):699-718. PubMed ID: 1200027
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  • 6. Partial duplication of 3q and distal deletion of 10q inherited from a maternal balanced translocation.
    Su PH, Chen JY, Chen SJ, Hung HM.
    J Formos Med Assoc; 2004 Nov 15; 103(11):853-7. PubMed ID: 15549153
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  • 7. Duplication 3q syndrome: molecular delineation of the critical region.
    Aqua MS, Rizzu P, Lindsay EA, Shaffer LG, Zackai EH, Overhauser J, Baldini A.
    Am J Med Genet; 1995 Jan 02; 55(1):33-7. PubMed ID: 7702094
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  • 8. A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion.
    Rodríguez L, Bhatt SS, García-Castro M, Plasencia A, Fernández-Toral J, Abarca E, de Bello Cioffi M, Liehr T.
    Gene; 2014 Feb 10; 535(2):165-9. PubMed ID: 24316129
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  • 10. Familial complex 3q;10q rearrangement unraveled by subtelomeric FISH analysis.
    Battaglia A, Novelli A, Ceccarini C, Carey JC.
    Am J Med Genet A; 2006 Jan 15; 140(2):144-50. PubMed ID: 16353244
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  • 12. Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.
    Zafra de la Rosa G, Venegas-Vega CA, Monroy N, Contreras-Bucio G, Friedrich U, Houman M, Saad A, Fernández P, Kofman-Alfaro S, Cervantes A.
    Am J Med Genet A; 2005 Jul 30; 136(3):259-64. PubMed ID: 15957183
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  • 13. Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5) (p13.1----p15.3).
    Kleczkowska A, Fryns JP, Moerman P, Vandenberghe K, Van den Berghe H.
    Clin Genet; 1987 Jul 30; 32(1):49-56. PubMed ID: 3621654
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  • 15. Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent-1 segregants.
    Kozma C, Slavotinek AM, Meck JM.
    Am J Med Genet A; 2004 Jan 15; 124A(2):118-28. PubMed ID: 14699608
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  • 16. 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.
    Chen CP, Lin CJ, Chen YY, Wang LK, Chern SR, Wu PS, Su JW, Chen LF, Town DD, Pan CW, Wang W.
    Gene; 2013 Dec 10; 532(1):80-6. PubMed ID: 24055486
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  • 19. Patient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome.
    Angle B, Yen F, Hersh JH, Gowans G.
    Am J Med Genet A; 2003 Feb 01; 116A(4):376-80. PubMed ID: 12522795
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