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Journal Abstract Search

166 related items for PubMed ID: 18205863

  • 1. Segregation analysis in X-linked ichthyosis: paternal transmission of the affected X-chromosome.
    Toral-Lopez J, González-Huerta LM, Cuevas-Covarrubias SA.
    Br J Dermatol; 2008 Apr; 158(4):818-20. PubMed ID: 18205863
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  • 2. Analysis of the VCX3A, VCX2 and VCX3B genes shows that VCX3A gene deletion is not sufficient to result in mental retardation in X-linked ichthyosis.
    Cuevas-Covarrubias SA, González-Huerta LM.
    Br J Dermatol; 2008 Mar; 158(3):483-6. PubMed ID: 18076704
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  • 4. Deletion pattern of the STS gene in X-linked ichthyosis in a Mexican population.
    Jimenez Vaca AL, Valdes-Flores Mdel R, Rivera-Vega MR, González-Huerta LM, Kofman-Alfaro SH, Cuevas-Covarrubias SA.
    Mol Med; 2001 Dec; 7(12):845-9. PubMed ID: 11844872
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  • 5. Deletion of distal promoter of VCXA in a patient with X-linked ichthyosis associated with borderline mental retardation.
    Hosomi N, Oiso N, Fukai K, Hanada K, Fujita H, Ishii M.
    J Dermatol Sci; 2007 Jan; 45(1):31-6. PubMed ID: 17113756
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  • 6. Xp22.3 interstitial deletion: a recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation.
    Ben Khelifa H, Soyah N, Ben-Abdallah-Bouhjar I, Gritly R, Sanlaville D, Elghezal H, Saad A, Mougou-Zerelli S.
    Gene; 2013 Sep 25; 527(2):578-83. PubMed ID: 23791652
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  • 9. [Investigation of steroid sulfatase gene in two pedigrees with X-linked ichthyosis].
    Liu A, Xiao SX, Tan SS, Jiao T, Liu Y, Li XL, Zhou SN.
    Di Yi Jun Yi Da Xue Xue Bao; 2005 Aug 25; 25(8):1023-5. PubMed ID: 16109567
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  • 10. 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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  • 12. Analysis of the STS gene in 40 patients with recessive X-linked ichthyosis: a high frequency of partial deletions in a Spanish population.
    Cañueto J, Ciria S, Hernández-Martín A, Unamuno P, González-Sarmiento R.
    J Eur Acad Dermatol Venereol; 2010 Oct 06; 24(10):1226-9. PubMed ID: 20236202
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  • 13. 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 06; 39(3):182-7. PubMed ID: 10759956
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  • 14. Atypical X-linked ichthyosis in a patient with a large deletion involving the steroid sulfatase (STS) gene.
    Gonzalez-Huerta L, Mendiola-Jimenez J, Del Moral-Stevenel M, Rivera-Vega M, Cuevas-Covarrubias S.
    Int J Dermatol; 2009 Feb 06; 48(2):142-4. PubMed ID: 19200188
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  • 15. Deletion pattern of the steroid sulphatase gene in Japanese patients with X-linked ichthyosis.
    Saeki H, Kuwata S, Nakagawa H, Shimada S, Tamaki K, Ishibashi Y.
    Br J Dermatol; 1998 Jul 06; 139(1):96-8. PubMed ID: 9764155
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  • 16. 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 Jul 06; 6(2):103-7. PubMed ID: 7546451
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  • 17. The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray.
    Hand JL, Runke CK, Hodge JC.
    J Am Acad Dermatol; 2015 Apr 06; 72(4):617-27. PubMed ID: 25659225
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  • 18. X-linked recessive ichthyosis.
    Hazan C, Orlow SJ, Schaffer JV.
    Dermatol Online J; 2005 Dec 30; 11(4):12. PubMed ID: 16403384
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