232 related articles for article (PubMed ID: 17113756)
1. 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
[TBL] [Abstract][Full Text] [Related]
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
[TBL] [Abstract][Full Text] [Related]
3. 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; 527(2):578-83. PubMed ID: 23791652
[TBL] [Abstract][Full Text] [Related]
4. 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; 9(10):1192-6. PubMed ID: 20941942
[TBL] [Abstract][Full Text] [Related]
5. [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(8):1023-5. PubMed ID: 16109567
[TBL] [Abstract][Full Text] [Related]
6. 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; 14(13):1795-803. PubMed ID: 15888481
[TBL] [Abstract][Full Text] [Related]
7. 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; 48(2):142-4. PubMed ID: 19200188
[TBL] [Abstract][Full Text] [Related]
8. 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
[TBL] [Abstract][Full Text] [Related]
9. [Multiplex quantitative PCR detection for female carrier in an X-linked ichthyosis family].
Zhu HY; Li HB; Wu LQ; Zhu XY; Li J; Yang Y; Zhu RF; Wu X; Duan HL; Zhang Y; Hu YL
Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3246-9. PubMed ID: 19159546
[TBL] [Abstract][Full Text] [Related]
10. The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray.
Hand JL; Runke CK; Hodge JC
J Am Acad Dermatol; 2015 Apr; 72(4):617-27. PubMed ID: 25659225
[TBL] [Abstract][Full Text] [Related]
11. 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; 67(4):367-8. PubMed ID: 15733277
[No Abstract] [Full Text] [Related]
12. 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; 39(3):182-7. PubMed ID: 10759956
[TBL] [Abstract][Full Text] [Related]
13. Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations.
Ramesh R; Chen H; Kukula A; Wakeling EL; Rustin MH; McLean WH
J Dermatol Sci; 2011 Dec; 64(3):159-62. PubMed ID: 21945601
[TBL] [Abstract][Full Text] [Related]
14. 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; 45(8):519-24. PubMed ID: 18413370
[TBL] [Abstract][Full Text] [Related]
15. 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; 24(10):1226-9. PubMed ID: 20236202
[TBL] [Abstract][Full Text] [Related]
16. 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; 75(5):340-2. PubMed ID: 8615047
[TBL] [Abstract][Full Text] [Related]
17. STS gene in a pedigree with X-linked ichthyosis.
Liu A; Xiao S; Tan S; Lei X; Zhang J; Jiao T; Liu Y
J Huazhong Univ Sci Technolog Med Sci; 2005; 25(4):468-9. PubMed ID: 16196306
[TBL] [Abstract][Full Text] [Related]
18. Prenatal in situ hybridization test for deleted steroid sulfatase gene.
Lebo RV; Lynch ED; Golbus MS; Flandermeyer RR; Yen PH; Shapiro LJ
Am J Med Genet; 1993 Jul; 46(6):652-8. PubMed ID: 8362907
[TBL] [Abstract][Full Text] [Related]
19. Genetic analysis of a 12-year-old boy with X-linked ichthyosis in association with sclerosing glomerulonephritis.
Song Y; Chen J; Yi Z; Dang X; Cheng D; Wu X; Tan Y
Mol Med Rep; 2013 Oct; 8(4):1183-7. PubMed ID: 23939749
[TBL] [Abstract][Full Text] [Related]
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; 59(2):143-8. PubMed ID: 8588575
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
