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Journal Abstract Search

177 related items for PubMed ID: 6733951

  • 1. Trisomy 7 and Potter syndrome.
    Pflueger SM, Scott CI, Moore CM.
    Clin Genet; 1984 Jun; 25(6):543-8. PubMed ID: 6733951
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  • 3. Trisomy 9 mosaicism in a girl with multiple malformations.
    Diaz-Mares L, Molina B, Carnevale A.
    Ann Genet; 1990 Jun; 33(3):165-8. PubMed ID: 2288462
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  • 4. Trisomy 9 syndrome.
    Qazi QH, Masakawa A, Madahar C, Ehrlich R.
    Clin Genet; 1977 Oct; 12(4):221-6. PubMed ID: 912938
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  • 5. Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring.
    Jalal SM, Martin JA, Benjamin TR, Kukolich MK, Townsend-Parcham JK.
    Ann Genet; 1990 Oct; 33(3):173-5. PubMed ID: 2288463
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  • 6. Chromosomal mosaicism in the Killian/Teschler-Nicola syndrome.
    Raffel LJ, Mohandas T, Rimoin DL.
    Am J Med Genet; 1986 Aug; 24(4):607-11. PubMed ID: 3740095
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  • 8. [Potter syndrome (kidney agenesis) with chromosome abnormalities in the patient and mosaicism in the father].
    Ferrandez A, Schmid W.
    Helv Paediatr Acta; 1971 Jun; 26(2):210-4. PubMed ID: 5139247
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  • 10. Trisomy 14 mosaicism syndrome.
    Lipson MH.
    Am J Med Genet; 1987 Mar; 26(3):541-4. PubMed ID: 3565467
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  • 14. Phenotype of partial trisomy 8 (p21 leads to qter) in two unrelated patients with de novo translocation.
    Sachs ES, van Waveren G.
    J Med Genet; 1981 Jun; 18(3):204-8. PubMed ID: 7241543
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  • 15. [Trisomy 9p - clinical and cytogenetic syndrome].
    Hitrec V, Zergollern L.
    Acta Med Iugosl; 1979 Jun; 33(2):169-82. PubMed ID: 506795
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  • 18. Trisomy 8 mosaicism syndrome. Report of monozygotic twins.
    Reyes PG, Hsu LY, Strauss L, Rose J, Hirschhorn K.
    Clin Genet; 1978 Aug; 14(2):90-7. PubMed ID: 567548
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  • 19. Mosaicism for duplication 12q (12q13-->q24.2) in a dysmorphic male infant.
    Dixon JW, Costa T, Teshima IE.
    J Med Genet; 1993 Jan; 30(1):70-2. PubMed ID: 8423612
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