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Journal Abstract Search

200 related items for PubMed ID: 422195

  • 1. Trisomy 10p due to a de novo t(10p;13p).
    Aller V, Abrisqueta JA, Pérez-Castillo A, del Mazo J, Martín-Lucas MA, de Torres ML.
    Hum Genet; 1979 Jan 25; 46(2):129-34. PubMed ID: 422195
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  • 5. Unbalanced karyotype with normal phenotype in a family with translocation (8;13)(p21;q22).
    Bröcker-Vriends AH, van de Kamp JJ, Geraedts JP, Bos SE, Nijenhuis TA.
    Clin Genet; 1985 May 25; 27(5):487-95. PubMed ID: 4006274
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  • 7. A severely retarded 18-year-old boy with tertiary partial trisomy 14.
    Smith A, den Dulk G, Elliott G.
    J Med Genet; 1980 Jun 25; 17(3):230-2. PubMed ID: 7401136
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  • 8. Partial trisomy 11q as the result of sporadic translocation.
    Lurie IW, Lazjuk GI, Usova YI, Gurevich DB.
    Hum Genet; 1979 Sep 02; 51(1):63-6. PubMed ID: 500093
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  • 11. Trisomy 10p, due to an unusual translocation.
    Orye E, Van Haesebrouck P, Van Coster R, Van Mele B.
    J Genet Hum; 1985 Jan 02; 33(1):63-6. PubMed ID: 3981144
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  • 13. A case of trisomy 22 with a probable Robertsonian translocation 21/22.
    Lalchev S, Tzancheva M, Markova R.
    Hum Genet; 1978 Dec 18; 45(2):219-23. PubMed ID: 738723
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  • 19. Banding identification of partial trisomy 15 and of 8/21 translocation.
    Wurster-Hill DH, Hoefnagel D.
    J Ment Defic Res; 1974 Jun 18; 18(2):139-44. PubMed ID: 4141377
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