146 related articles for article (PubMed ID: 9247725)
1. 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; 263(1):25-32. PubMed ID: 9247725
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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; 38(4):421-8. PubMed ID: 8186420
[TBL] [Abstract][Full Text] [Related]
4. 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; 72(4):415-6. PubMed ID: 9375723
[TBL] [Abstract][Full Text] [Related]
5. 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; 102(2):146-8. PubMed ID: 11477606
[TBL] [Abstract][Full Text] [Related]
6. Characterization of the deletion breakpoints in a patient with steroid sulfatase deficiency.
Yen PH; Ferrero GB; Chinault AC; Mohandas T; Ballabio A
Hum Mutat; 1994; 4(1):76-8. PubMed ID: 7951263
[No Abstract] [Full Text] [Related]
7. 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; 114(3):591-3. PubMed ID: 10692123
[TBL] [Abstract][Full Text] [Related]
8. Somatic and germinal mosaicism for the steroid sulfatase gene deletion in a steroid sulfatase deficiency carrier.
Cuevas-Covarrubias SA; Jiménez-Vaca AL; González-Huerta LM; Valdes-Flores M; Del Refugio Rivera-Vega M; Maya-Nunez G; Kofman-Alfaro SH
J Invest Dermatol; 2002 Oct; 119(4):972-5. PubMed ID: 12406347
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Most "sporadic" cases of X-linked ichthyosis are not de novo mutations.
Cuevas-Covarrubias SA; Valdes-Flores M; Orozco Orozco E; Díaz-Zagoya JC; Kofman-Alfaro SH
Acta Derm Venereol; 1999 Mar; 79(2):143-4. PubMed ID: 10228635
[TBL] [Abstract][Full Text] [Related]
11. 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; 109(2):244-5. PubMed ID: 9242515
[TBL] [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. 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]
14. [Gene deletion of X-linked ichthyosis].
Li M
Zhonghua Yi Xue Za Zhi; 1992 Apr; 72(4):210-2, 254. PubMed ID: 1327447
[TBL] [Abstract][Full Text] [Related]
15. [Biochemical study on steroid sulfatase and its clinical application to the obstetrics and gynecology].
Sugawara T
Hokkaido Igaku Zasshi; 1992 Jul; 67(4):552-62. PubMed ID: 1427599
[TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of X-linked ichthyosis in Japan.
Sugawara T; Fujimoto Y; Fujimoto S
Horm Res; 2001; 56(5-6):182-7. PubMed ID: 11910205
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Prenatal diagnosis of X-linked ichthyosis using molecular cytogenetics.
Santolaya-Forgas J; Cohen L; Vengalil S; Field F; Rodriguez A; McCorquadale M; McCorquadale DJ
Fetal Diagn Ther; 1997; 12(1):36-9. PubMed ID: 9101220
[TBL] [Abstract][Full Text] [Related]
19. PCR diagnosis of X-linked ichthyosis: identification of a novel mutation (E560P) of the steroid sulfatase gene.
Sugawara T; Shimizu H; Hoshi N; Fujimoto Y; Nakajima A; Fujimoto S
Hum Mutat; 2000 Mar; 15(3):296. PubMed ID: 10679952
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
