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Journal Abstract Search

243 related items for PubMed ID: 7794563

  • 1. Interstitial deletion of the short arm of chromosome 8: report of a patient and review of the literature.
    Plomp AS, Schrander-Stumpel CT, Engelen JJ, Sijstermans JM, Loneus WH, Fryns JP.
    Genet Couns; 1995; 6(1):55-60. PubMed ID: 7794563
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  • 2. Interstitial deletion of 8q13.3-->22.1 associated with craniosynostosis.
    Fryburg JS, Golden WL.
    Am J Med Genet; 1993 Mar 01; 45(5):638-41. PubMed ID: 7681252
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  • 7. Moderate mental retardation and mild dysmorphic syndrome in proximal 7q interstitial deletion.
    Fryns JP, Kleczkowska A, Van den Berghe H.
    Ann Genet; 1987 Mar 01; 30(2):111-2. PubMed ID: 3499842
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  • 9. Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant.
    Gillar PJ, Kaye CI, Ryan SG, Moore CM.
    Am J Med Genet; 1992 Sep 15; 44(2):138-41. PubMed ID: 1456281
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  • 10. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.
    Taysi K, Strauss AW, Yang V, Padmalatha C, Marshall RE.
    Ann Genet; 1982 Sep 15; 25(3):141-4. PubMed ID: 6982660
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  • 11. Interstitial deletion of the long arm of chromosome 2: a case report and review of the literature.
    Takahashi Y, Narahara K, Kikkawa K, Wakita Y, Kimura S, Murakami M, Kasai R, Kimoto H.
    Jinrui Idengaku Zasshi; 1985 Dec 15; 30(4):297-305. PubMed ID: 3869838
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  • 14. Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies.
    Back E, Hertel C, Vogel W, Bettecken F, Thiesen M.
    Ann Genet; 1977 Dec 15; 20(4):294-6. PubMed ID: 305761
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  • 16. Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome.
    Fryns JP, Yang-Aisheng, Kleczkowska A, Lemmens F, Vandecasseye W, van den Berghe H.
    Ann Genet; 1989 Dec 15; 32(1):59-61. PubMed ID: 2751251
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  • 17. Interstitial deletion 8p21.3----p23.1 in a 6-year-old girl.
    Morrison PJ, Jones J, Nevin NC.
    Am J Med Genet; 1992 Mar 01; 42(5):678-80. PubMed ID: 1632437
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  • 18. Terminal deletion 4q in a severely retarded boy.
    de Michelena MI, Campos PJ.
    Am J Med Genet; 1989 Jun 01; 33(2):228-30. PubMed ID: 2764033
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  • 20. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
    Bremer A, Schoumans J, Nordenskjöld M, Anderlid BM, Giacobini M.
    Eur J Med Genet; 2009 Jun 01; 52(5):358-62. PubMed ID: 19576304
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