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Journal Abstract Search

227 related items for PubMed ID: 1536169

  • 41. Partial duplication of distal 17q.
    Bridge J, Sanger W, Mosher G, Buehler B, Hearty C, Olney A, Fordyce R.
    Am J Med Genet; 1985 Oct; 22(2):229-35. PubMed ID: 4050855
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  • 42. Partial trisomy of chromosome 18 (pter leads to q11): a discussion on the identification of the critical segment.
    San Martin V, Fernandez-Novoa C, Hevia A, Novales A, Fornell J, Galera H.
    Ann Genet; 1981 Oct; 24(4):248-50. PubMed ID: 6977308
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  • 43. Duplication 11 (q22----qter) in an infant. A case report with review.
    Greig F, Rosenfeld W, Verma RS, Babu KA, David K.
    Ann Genet; 1985 Oct; 28(3):185-8. PubMed ID: 3879155
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  • 48. Branchial arch anomalies in trisomy 18.
    Verloes A, Seret N, Bernier V, Gonzales M, Herens C, Koulischer L.
    Ann Genet; 1991 Oct; 34(1):22-4. PubMed ID: 1952786
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  • 50. Dup(1q)(q42-->qter) syndrome: case report and review of literature.
    Kennerknecht I, Barbi G, Rodens K.
    Am J Med Genet; 1993 Dec 01; 47(8):1157-60. PubMed ID: 7507296
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  • 51. A case of insertional translocation resulting in partial trisomy 16p.
    Kokalj-Vokac N, Medica I, Zagorac A, Zagradisnik B, Erjavec A, Gregoric A.
    Ann Genet; 2000 Dec 01; 43(3-4):131-5. PubMed ID: 11164194
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  • 53. Type and contretype signs in monosomy and trisomy 9p. On a case 46,XY, del (9) (pter yields p12:).
    Hernandez A, Rivera H, Jiménez-Sainz M, Fragoso R, Nazara Z, Cantu JM.
    Ann Genet; 1979 Dec 01; 22(3):155-7. PubMed ID: 316671
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  • 55. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.
    Wolff DJ, Schwartz MF, Cohen MM, Schwartz S.
    Am J Med Genet; 1993 Jun 15; 46(5):520-3. PubMed ID: 8322813
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  • 57. Secondary trisomy or mosaic "tetrasomy" 8p.
    Robinow M, Haney N, Chen H, Sorauf T, Van Dyke DL, Babu VR, Powell S, Maliszewski W, Guerin S, Landers JW.
    Am J Med Genet; 1989 Mar 15; 32(3):320-4. PubMed ID: 2729351
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  • 58. Endoreduplications in a family with a reciprocal translocation (9q;16p).
    Pinel I, Urioste M, Martinez-Frias ML, Gomar JL.
    Clin Genet; 1990 Nov 15; 38(5):399-400. PubMed ID: 2282723
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  • 59. Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndrome.
    Fryns JP.
    Genet Couns; 1998 Nov 15; 9(3):229-30. PubMed ID: 9777347
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  • 60. 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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