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Journal Abstract Search

166 related items for PubMed ID: 9375723

  • 1. X-linked ichthyosis in Mexico: high frequency of deletions in the steroid sulfatase encoding gene.
    Cuevas-Covarrubias SA, Kofman-Alfaro SH, Maya-Núñez G, Díaz-Zagoya JC, Orozco Orozco E.
    Am J Med Genet; 1997 Nov 12; 72(4):415-6. PubMed ID: 9375723
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  • 3. A study of the steroid sulfatase gene in families with X-linked ichthyosis using polymerase chain reaction.
    Nomura K, Nakano H, Umeki K, Harada K, Kon A, Tamai K, Sawamura D, Hashimoto I.
    Acta Derm Venereol; 1995 Sep 12; 75(5):340-2. PubMed ID: 8615047
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  • 4. Deletion of exons 1-5 of the STS gene causing X-linked ichthyosis.
    Valdes-Flores M, Kofman-Alfaro SH, Vaca AL, Cuevas-Covarrubias SA.
    J Invest Dermatol; 2001 Mar 12; 116(3):456-8. PubMed ID: 11231321
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  • 5. Steroid sulfatase deficiency in Japanese patients: characterization of X-linked ichthyosis by using polymerase chain reaction.
    Sugawara T, Honke K, Fujimoto S, Makita A.
    Jpn J Hum Genet; 1993 Dec 12; 38(4):421-8. PubMed ID: 8186420
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  • 6. Mutation report: a novel partial deletion of exons 2-10 of the STS gene in recessive X-linked ichthyosis.
    Valdes-Flores M, Kofman-Alfaro SH, Vaca AL, Cuevas-Covarrubias SA.
    J Invest Dermatol; 2000 Mar 12; 114(3):591-3. PubMed ID: 10692123
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  • 7. A novel point mutation in the steroid sulfatase gene in X-linked ichthyosis.
    Morita E, Katoh O, Shinoda S, Hiragun T, Tanaka T, Kameyoshi Y, Yamamoto S.
    J Invest Dermatol; 1997 Aug 12; 109(2):244-5. PubMed ID: 9242515
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  • 8. Carrier identification by FISH analysis in isolated cases of X-linked ichthyosis.
    Valdes-Flores M, Kofman-Alfaro SH, Jimenez-Vaca AL, Cuevas-Covarrubias SA.
    Am J Med Genet; 2001 Aug 01; 102(2):146-8. PubMed ID: 11477606
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  • 9. Deletion patterns of the STS gene and flanking sequences in Israeli X-linked ichthyosis patients and carriers: analysis by polymerase chain reaction and fluorescence in situ hybridization techniques.
    Aviram-Goldring A, Goldman B, Netanelov-Shapira I, Chen-Shtoyerman R, Zvulunov A, Tal O, Ilan T, Peleg L.
    Int J Dermatol; 2000 Mar 01; 39(3):182-7. PubMed ID: 10759956
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  • 10. Diagnosis of a deletion of steroid sulfatase by polymerase chain reaction and high-performance liquid chromatography.
    Sugawara T, Iwaki M, Fujimoto S.
    Clin Chim Acta; 1997 Jul 04; 263(1):25-32. PubMed ID: 9247725
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  • 15. Steroid sulfatase activity in leukocytes: a comparative study in 45,X; 46,Xi(Xq) and carriers of steroid sulfatase deficiency.
    Miranda-Duarte A, Valdés-Flores M, Miranda-Zamora R, Díaz-Zagoya JC, Kofman-Alfaro SH, Cuevas-Covarrubias SA.
    Biochem Mol Biol Int; 1999 Jan 04; 47(1):137-42. PubMed ID: 10092953
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  • 16. Molecular analysis of X-linked ichthyosis in Japan.
    Sugawara T, Fujimoto Y, Fujimoto S.
    Horm Res; 2001 Jan 04; 56(5-6):182-7. PubMed ID: 11910205
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  • 17. The biochemical identification of carrier state in mothers of sporadic cases of X-linked recessive ichthyosis.
    Cuevas-Covarrubias SA, Kofman-Alfaro S, Orozco Orozco E, Diaz-Zagoya JC.
    Genet Couns; 1995 Jan 04; 6(2):103-7. PubMed ID: 7546451
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  • 18. An atypical contiguous gene syndrome: molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis.
    Maya-Nuñez G, Torres L, Ulloa-Aguirre A, Zenteno JC, Cuevas-Covarrubias S, Saavedra-Ontiveros D, Kofman-Alfaro S, Méndez JP.
    Clin Endocrinol (Oxf); 1999 Feb 04; 50(2):157-62. PubMed ID: 10396356
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  • 19. [Gene deletion of X-linked ichthyosis].
    Li M.
    Zhonghua Yi Xue Za Zhi; 1992 Apr 04; 72(4):210-2, 254. PubMed ID: 1327447
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  • 20. X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studies.
    Robledo R, Melis P, Schillinger E, Casciano I, Balazs I, Rinaldi A, Siniscalco M, Filippi G.
    Am J Med Genet; 1995 Nov 06; 59(2):143-8. PubMed ID: 8588575
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