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180 related items for PubMed ID: 18076704

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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 25; 45(1):31-6. PubMed ID: 17113756
    [Abstract] [Full Text] [Related]

  • 4. 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 25; 158(4):818-20. PubMed ID: 18205863
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  • 5. Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis.
    Van Esch H, Hollanders K, Badisco L, Melotte C, Van Hummelen P, Vermeesch JR, Devriendt K, Fryns JP, Marynen P, Froyen G.
    Hum Mol Genet; 2005 Jul 01; 14(13):1795-803. PubMed ID: 15888481
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  • 6. 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 01; 7(12):845-9. PubMed ID: 11844872
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  • 7. Xp22.3 microdeletion including VCX-A and VCX-B1 genes in an X-linked ichthyosis family: no difference in deletion size for patients with and without mental retardation.
    Lesca G, Sinilnikova O, Theuil G, Blanc J, Edery P, Till M.
    Clin Genet; 2005 Apr 01; 67(4):367-8. PubMed ID: 15733277
    [No Abstract] [Full Text] [Related]

  • 8. 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 01; 48(2):142-4. PubMed ID: 19200188
    [Abstract] [Full Text] [Related]

  • 9. Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect.
    Macarov M, Zeigler M, Newman JP, Strich D, Sury V, Tennenbaum A, Meiner V.
    J Intellect Disabil Res; 2007 May 01; 51(Pt 5):329-33. PubMed ID: 17391250
    [Abstract] [Full Text] [Related]

  • 10. The detection of steroid sulfatase gene deletion (STS) in Egyptian males with X-linked ichthyosis.
    Abdel-Hamed MF, Hussein HA, Helmy NA, Elsaie ML.
    J Drugs Dermatol; 2010 Oct 01; 9(10):1192-6. PubMed ID: 20941942
    [Abstract] [Full Text] [Related]

  • 11. [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 01; 25(8):1023-5. PubMed ID: 16109567
    [Abstract] [Full Text] [Related]

  • 12. Normal intelligence and social interactions in a male patient despite the deletion of NLGN4X and the VCX genes.
    Mochel F, Missirian C, Reynaud R, Moncla A.
    Eur J Med Genet; 2008 Aug 01; 51(1):68-73. PubMed ID: 18194880
    [Abstract] [Full Text] [Related]

  • 13. 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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  • 18. 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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  • 19. X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits.
    Kent L, Emerton J, Bhadravathi V, Weisblatt E, Pasco G, Willatt LR, McMahon R, Yates JR.
    J Med Genet; 2008 Aug 12; 45(8):519-24. PubMed ID: 18413370
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