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Journal Abstract Search

148 related items for PubMed ID: 8588585

  • 1. Two craniosynostotic patients with 11q deletions, and review of 48 cases.
    Lewanda AF, Morsey S, Reid CS, Jabs EW.
    Am J Med Genet; 1995 Nov 06; 59(2):193-8. PubMed ID: 8588585
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  • 2. 11q- syndrome: three cases and a review of the literature.
    Leegte B, Kerstjens-Frederikse WS, Deelstra K, Begeer JH, van Essen AJ.
    Genet Couns; 1999 Nov 06; 10(3):305-13. PubMed ID: 10546104
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  • 3. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M, Hemly NA, Zaki MS.
    Genet Couns; 2007 Nov 06; 18(2):217-26. PubMed ID: 17710874
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  • 4. A patient with partial duplication 2q and partial deficiency 11q.
    Ho CK, Henderson KC, Bowyer FP, Eilers KB, Andrews LG.
    Am J Med Genet; 1987 Nov 06; 28(3):575-9. PubMed ID: 3322008
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  • 7. 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 Nov 06; 22(4):417-23. PubMed ID: 22303803
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  • 8. Partial monosomy 11q and trisomy 12q: variable expression in two siblings.
    Lukusa T, Holvoet M, Vermeesch JR, Devriendt K, Fryns JP.
    Genet Couns; 2003 Nov 06; 14(2):155-64. PubMed ID: 12872809
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  • 9. 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 Nov 06; 18(2):201-7. PubMed ID: 17710872
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  • 10. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
    Cousineau AJ, Higgins JV, Scott-Emuakpor AB, Mody G.
    Am J Med Genet; 1983 Jan 06; 14(1):29-35. PubMed ID: 6829609
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  • 11. 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 06; 16(4):231-9. PubMed ID: 17786114
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  • 12. Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly.
    Jehee FS, Johnson D, Alonso LG, Cavalcanti DP, de Sá Moreira E, Alberto FL, Kok F, Kim C, Wall SA, Jabs EW, Boyadjiev SA, Wilkie AO, Passos-Bueno MR.
    Clin Genet; 2005 Jun 06; 67(6):503-10. PubMed ID: 15857417
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  • 13. [4p trisomy secondary to paternal translocation t(4p-;15q+)].
    Saad A, Khelif M, Kharrat H, Bouzakoura C.
    Ann Pediatr (Paris); 1991 May 06; 38(5):350-4. PubMed ID: 1872531
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  • 14. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
    Hegmann KM, Spikes AS, Orr-Urtreger A, Shaffer LG.
    Am J Med Genet; 1996 Jan 02; 61(1):10-5. PubMed ID: 8741910
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