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Journal Abstract Search

402 related items for PubMed ID: 7856655

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  • 3. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
    Merlob P, Kohn G, Litwin A, Nissenkorn I, Katznelson MB, Reisner SH.
    Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
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  • 4. Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.
    Angle B, Yen F, Hersh JH, Gowans G, Barch M.
    Am J Med Genet; 2002 Aug 15; 111(3):307-12. PubMed ID: 12210328
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  • 8. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 15; 26(2):138-46. PubMed ID: 16470734
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  • 9. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
    Chen Z, Grebe TA, Guan XY, Notohamiprodjo M, Nutting PJ, Stone JF, Trent JM, Sandberg AA.
    Am J Med Genet; 1997 Aug 08; 71(2):160-6. PubMed ID: 9217215
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  • 10. Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25).
    Makita Y, Masuno M, Imaizumi K, Yamashita S, Ohba S, Ito D, Kuroki Y.
    Am J Med Genet; 1995 May 22; 57(1):19-21. PubMed ID: 7645592
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  • 11. Duplication of distal 19q: clinical report and review.
    Boyd E, Grass FS, Parke JC, Knutson K, Stevenson RE.
    Am J Med Genet; 1992 Feb 01; 42(3):326-30. PubMed ID: 1536172
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  • 12. 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 01; 27(3):687-92. PubMed ID: 3631140
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  • 13. Duplication of distal 22q.
    Abeliovich D, Maor E, Bashan N, Carmi R.
    Am J Med Genet; 1989 Mar 01; 32(3):346-9. PubMed ID: 2729354
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  • 14. Partial 4q duplication due to inherited der(20), t(4;20)(q25;q13)mat.
    Sparkes RS, Francke U, Muller H, Toomey K.
    Ann Genet; 1977 Mar 01; 20(1):31-5. PubMed ID: 302670
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  • 15. De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.
    Chitayat D, Fagerstrom CL, Kalousek DK, Rootman J, Taylor GP, Hall JG.
    Am J Med Genet; 1989 Jan 01; 32(1):36-41. PubMed ID: 2495721
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  • 16. Complex chromosome rearrangements and congenital anomalies.
    Kousseff BG, Nichols P, Essig YP, Miller K, Weiss A, Tedesco TA.
    Am J Med Genet; 1987 Apr 01; 26(4):771-82. PubMed ID: 3591822
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  • 17. Confirmation of a cryptic unbalanced translocation using whole chromosome fluorescence in situ hybridization.
    Mewar R, Kline AD, Jackson L, Overhauser J.
    Am J Med Genet; 1992 Nov 01; 44(4):477-81. PubMed ID: 1442891
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  • 18. Monosomy 11q: report of two familial cases and review of the literature.
    Hustinx R, Verloes A, Grattagliano B, Herens C, Jamar M, Soyeur D, Schaaps JP, Koulischer L.
    Am J Med Genet; 1993 Sep 01; 47(3):312-7. PubMed ID: 8135272
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  • 19. 10p duplication characterized by fluorescence in situ hybridization.
    Wiktor A, Feldman GL, Kratkoczki P, Ditmars DM, Van Dyke DL.
    Am J Med Genet; 1994 Sep 01; 52(3):315-8. PubMed ID: 7528972
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  • 20. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
    Schürmann M, Wethling H, Niemeyer ML, Schwinger E.
    Klin Padiatr; 1987 Sep 01; 199(1):27-31. PubMed ID: 2435950
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