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Journal Abstract Search

116 related items for PubMed ID: 1119458

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  • 3. Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2.
    Reardon W, McManus SP, Summers D, Winter RM.
    Am J Med Genet; 1993 Oct 01; 47(5):633-6. PubMed ID: 8266988
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  • 5. [Familial acrocephalosyndactylia with features of the Saethre-Chotzen syndrome].
    Kopyść Z, Kulczyk B, Ryzko J, Gura C, Stańska M, Kowalski K.
    Pediatr Pol; 1979 Jul 01; 54(7):769-72. PubMed ID: 530768
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  • 9. The Saethre-Chotzen syndrome.
    Kreiborg S, Pruzansky S, Pashayan H.
    Teratology; 1972 Dec 01; 6(3):287-94. PubMed ID: 4643612
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  • 13. Saethre-Chotzen syndrome and hyper IgE syndrome in a patient with a novel 11 bp deletion of the TWIST gene.
    Boeck A, Kosan C, Ciznar P, Kunz J.
    Am J Med Genet; 2001 Nov 15; 104(1):53-6. PubMed ID: 11746028
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  • 14. Clinical and genetic analysis of patients with Saethre-Chotzen syndrome.
    de Heer IM, de Klein A, van den Ouweland AM, Vermeij-Keers C, Wouters CH, Vaandrager JM, Hovius SE, Hoogeboom JM.
    Plast Reconstr Surg; 2005 Jun 15; 115(7):1894-902; discussion 1903-5. PubMed ID: 15923834
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  • 17. Possible genetic heterogeneity in the Saethre-Chotzen syndrome.
    Ma HW, Lajeunie E, de Parseval N, Munnich A, Renier D, Le Merrer M.
    Hum Genet; 1996 Aug 15; 98(2):228-32. PubMed ID: 8698349
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  • 18. [Association of chronic tubulointerstitial nephropathy and Saethre-Chotzen syndrome. A family case].
    Fontaine G, Voultoury-Jensen P, Toursel F, Walbaum R, Farriaux JP.
    Ann Pediatr (Paris); 1976 Dec 02; 23(12):777-83. PubMed ID: 16106896
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  • 20. A family with the Saethre-Chotzen syndrome.
    Bianchi E, Aricŏ M, Podestă AF, Grana M, Fiori P, Beluffi G.
    Am J Med Genet; 1985 Dec 02; 22(4):649-58. PubMed ID: 4073118
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