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Journal Abstract Search

402 related items for PubMed ID: 7856655

  • 1. 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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  • 2. Jumping translocation in a newborn boy with dup(4q) and severe hydrops fetalis.
    Duval E, van den Enden A, Vanhaesebrouck P, Speleman F.
    Am J Med Genet; 1994 Aug 15; 52(2):214-7. PubMed ID: 7802011
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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 15; 32(1):22-6. PubMed ID: 2705479
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  • 6. Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomalies.
    Mohammed FM, Farag TI, Gunawardana SS, al-Digashim DD, al-Awadi SA, al-Othman SA, Sundareshan TS.
    Am J Med Genet; 1989 Mar 15; 32(3):353-5. PubMed ID: 2729356
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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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  • 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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  • 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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  • 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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