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PUBMED FOR HANDHELDS

Journal Abstract Search


306 related items for PubMed ID: 912938

  • 1. 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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  • 4. Clinical delineation of trisomy 9 syndrome.
    Katayama KP, Wilkinson EJ, Herrmann J, Glaspey JC, Agarwal AB, Roesler MR, Mattingly RF.
    Obstet Gynecol; 1980 Nov; 56(5):665-8. PubMed ID: 7432742
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  • 6. Natural history of mosaic trisomy 14 syndrome.
    Fujimoto A, Allanson J, Crowe CA, Lipson MH, Johnson VP.
    Am J Med Genet; 1992 Sep 15; 44(2):189-96. PubMed ID: 1456290
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  • 7. Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance.
    Dallaire L.
    J Med Genet; 1969 Jun 15; 6(2):113-20. PubMed ID: 4389828
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  • 8. Tetrasomy 9p confirmed by GALT.
    Balestrazzi P, Croci G, Frassi C, Franchi F, Giovannelli G.
    J Med Genet; 1983 Oct 15; 20(5):396-9. PubMed ID: 6644773
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  • 9. Partial trisomy 10q: a recognizable syndrome.
    Klep-de Pater JM, Bijlsma JB, de France HF, Leschot NJ, Duijndam-van den Berge M, van Hemel JO.
    Hum Genet; 1979 Jan 19; 46(1):29-40. PubMed ID: 429004
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  • 11. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22).
    Bowen P, Fitzgerald PH, Gardner RJ, Biederman B, Veale AM.
    Am J Med Genet; 1983 Apr 19; 14(4):635-46. PubMed ID: 6846399
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  • 14. [Trisomy 10 p. A previously reported case explained by binding].
    Turleau C, Doussau de Bazignan M, Roubin M, de Grouchy J.
    Ann Genet; 1976 Mar 19; 19(1):61-4. PubMed ID: 1084125
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  • 16. Trisomy 8 mosaicism syndrome.
    Fineman RM, Ablow RC, Howard RO, Albright J, Breg WR.
    Pediatrics; 1975 Nov 19; 56(5):762-7. PubMed ID: 1196733
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