168 related articles for article (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
[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. 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]
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
[TBL] [Abstract][Full Text] [Related]
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
[TBL] [Abstract][Full Text] [Related]
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; 527(2):578-83. PubMed ID: 23791652
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
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(8):1023-5. PubMed ID: 16109567
[TBL] [Abstract][Full Text] [Related]
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; 59(2):143-8. PubMed ID: 8588575
[TBL] [Abstract][Full Text] [Related]
11. 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]
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; 24(10):1226-9. PubMed ID: 20236202
[TBL] [Abstract][Full Text] [Related]
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; 39(3):182-7. PubMed ID: 10759956
[TBL] [Abstract][Full Text] [Related]
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; 48(2):142-4. PubMed ID: 19200188
[TBL] [Abstract][Full Text] [Related]
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; 139(1):96-8. PubMed ID: 9764155
[TBL] [Abstract][Full Text] [Related]
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; 6(2):103-7. PubMed ID: 7546451
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. X-linked recessive ichthyosis.
Hazan C; Orlow SJ; Schaffer JV
Dermatol Online J; 2005 Dec; 11(4):12. PubMed ID: 16403384
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. 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; 116(3):456-8. PubMed ID: 11231321
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
