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Journal Abstract Search

234 related items for PubMed ID: 8135272

  • 21. Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.
    Brown S, Gersen S, Anyane-Yeboa K, Warburton D.
    Am J Med Genet; 1993 Jan 01; 45(1):52-9. PubMed ID: 8418661
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  • 22. Deletion of terminal portion of 6q: report of a case with unusual malformations.
    Shen-Schwarz S, Hill LM, Surti U, Marchese S.
    Am J Med Genet; 1989 Jan 01; 32(1):81-6. PubMed ID: 2705486
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  • 25. De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21.
    Riegel M, Baumer A, Piram A, Ortolan D, Peres LC, Pina-Neto JM.
    Genet Couns; 2001 Jan 01; 12(1):69-75. PubMed ID: 11332980
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  • 26. Prenatal morphology of partial monosomy 18q.
    Lazjuk G, Zolotukhina T, Kirillova I, Lurie I, Novikova I, Abasheva G.
    Zentralbl Gynakol; 1987 Jan 01; 109(2):126-9. PubMed ID: 3577468
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  • 27. Branchial arch anomalies in trisomy 18.
    Verloes A, Seret N, Bernier V, Gonzales M, Herens C, Koulischer L.
    Ann Genet; 1991 Jan 01; 34(1):22-4. PubMed ID: 1952786
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  • 28. Familial translocation 5;14 resulting in an unbalanced offspring.
    Park JP, Edwards MJ, Moeschler JB, Marin-Padilla JM, Berg SZ, Wurster-Hill DH.
    Am J Med Genet; 1991 Jun 01; 39(3):362-6. PubMed ID: 1867291
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  • 30. [2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)].
    Morić-Petrović S, Laća Z, Krajgher A, Milośevic J.
    Ann Genet; 1976 Sep 01; 19(3):195-7. PubMed ID: 1086628
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  • 31. Familial t(11;13)(q21;q14) and the duplication 11q, 13q phenotype.
    Park JP, McDermet MK, Doody AM, Marin-Padilla JM, Moeschler JB, Wurster-Hill DH.
    Am J Med Genet; 1993 Jan 01; 45(1):46-8. PubMed ID: 8418658
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  • 32. 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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  • 37. [Partial monosomy 11q. A new case].
    Bresson JL, Noir A.
    Ann Genet; 1977 Mar 06; 20(1):63-6. PubMed ID: 302678
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  • 39. Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations.
    Ramer JC, Mowrey PN, Robins DB, Ligato S, Towfighi J, Ladda RL.
    Am J Med Genet; 1990 Nov 06; 37(3):392-400. PubMed ID: 2260571
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  • 40. 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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