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Journal Abstract Search

195 related items for PubMed ID: 1524409

  • 1. Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation.
    Sarda P, Lefort G, Devaux P, Humeau C, Rieu D.
    Ann Genet; 1992; 35(2):117-20. PubMed ID: 1524409
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  • 2. Translocation/duplication of 9p onto a duplicated 4q.
    Rivera H, Figuera LE, Vasquez AI.
    Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
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  • 3. Duplication of distal 22q.
    Abeliovich D, Maor E, Bashan N, Carmi R.
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
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  • 4. De novo partial 2p duplication with postmortem description.
    Monteleone PL, Blair JD, Graviss ER, Chen SC, Salvador A, Grzegocki JA, Monteleone JA.
    Am J Med Genet; 1981 Mar; 10(1):55-64. PubMed ID: 7197468
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  • 7. [Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication].
    Reichenbach H, Holland H, Thamm B, Theile T.
    Kinderarztl Prax; 1993 Oct; 61(7-8):291-5. PubMed ID: 8271681
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  • 8. Duplication 7p in a family with t(7;11): association with anomalies of the anterior cranial base.
    Odell JM, Siebert JR, Bradley C, Salk D.
    Am J Med Genet; 1987 Jul; 27(3):687-92. PubMed ID: 3631140
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  • 10. Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome.
    Kitsiou-Tzeli S, Hallett JJ, Atkins L, Latt SA, Holmes LB.
    Am J Med Genet; 1984 Aug; 18(4):725-9. PubMed ID: 6237580
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  • 11. Cytogenetic abnormalities in orthopedic patients.
    Cowell HR, Clark CE.
    Clin Orthop Relat Res; 1978 Sep; (135):4-14. PubMed ID: 152176
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  • 13. 8q22-->qter duplication in a child with multiple congenital malformations: case report.
    Sasiadek M, Stembalska A, Schlade K, Zych M.
    Med Sci Monit; 2000 Sep; 6(1):141-4. PubMed ID: 11208302
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  • 14. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
    Legare JM, Sekhon GS, Laxova R.
    Am J Med Genet; 1994 Nov 15; 53(3):216-21. PubMed ID: 7856655
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  • 17. Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.
    Lindgren V, Rosinsky B, Chin J, Berry-Kravis E.
    Am J Med Genet; 1994 Jan 01; 49(1):67-73. PubMed ID: 8172253
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  • 19. A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype.
    Park JP, McDermet MK, Moeschler JB, Wurster-Hill DH.
    Ann Genet; 1993 Jan 01; 36(4):217-20. PubMed ID: 8166428
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  • 20. Isochromosome-formation in chromosome 9.
    Miller K, Arslan-Kirchner M.
    Ann Genet; 1994 Jan 01; 37(2):78-81. PubMed ID: 7985983
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