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22. 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 [Abstract] [Full Text] [Related]
23. 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 [Abstract] [Full Text] [Related]
24. 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 01; 46(6):652-8. PubMed ID: 8362907 [Abstract] [Full Text] [Related]
25. [Gene deletion of X-linked ichthyosis]. Li M. Zhonghua Yi Xue Za Zhi; 1992 Apr 01; 72(4):210-2, 254. PubMed ID: 1327447 [Abstract] [Full Text] [Related]
26. 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 01; 116(3):456-8. PubMed ID: 11231321 [Abstract] [Full Text] [Related]
27. Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements. Yen PH, Li XM, Tsai SP, Johnson C, Mohandas T, Shapiro LJ. Cell; 1990 May 18; 61(4):603-10. PubMed ID: 2344613 [Abstract] [Full Text] [Related]
28. Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene? Fraser N, Ballabio A, Zollo M, Persico G, Craig I. Development; 1987 May 18; 101 Suppl():127-32. PubMed ID: 3503710 [Abstract] [Full Text] [Related]
29. Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis. Basler E, Grompe M, Parenti G, Yates J, Ballabio A. Am J Hum Genet; 1992 Mar 18; 50(3):483-91. PubMed ID: 1539590 [Abstract] [Full Text] [Related]
30. 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 [Abstract] [Full Text] [Related]
31. Human glucosamine-6-sulfatase cDNA reveals homology with steroid sulfatase. Robertson DA, Freeman C, Nelson PV, Morris CP, Hopwood JJ. Biochem Biophys Res Commun; 1988 Nov 30; 157(1):218-24. PubMed ID: 3196333 [Abstract] [Full Text] [Related]
32. Novel point mutations in the steroid sulfatase gene in patients with X-linked ichthyosis: transfection analysis using the mutated genes. Oyama N, Satoh M, Iwatsuki K, Kaneko F. J Invest Dermatol; 2000 Jun 30; 114(6):1195-9. PubMed ID: 10844566 [Abstract] [Full Text] [Related]
33. Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis. Ballabio A, Parenti G, Carrozzo R, Sebastio G, Andria G, Buckle V, Fraser N, Craig I, Rocchi M, Romeo G. Proc Natl Acad Sci U S A; 1987 Jul 30; 84(13):4519-23. PubMed ID: 3474618 [Abstract] [Full Text] [Related]
34. Low or absent unconjugated estriol in pregnancy: an indicator for steroid sulfatase deficiency detectable by fluorescence in situ hybridization and biochemical analysis. Kashork CD, Sutton VR, Fonda Allen JS, Schmidt DE, Likhite ML, Potocki L, O'Brien WE, Shaffer LG. Prenat Diagn; 2002 Nov 30; 22(11):1028-32. PubMed ID: 12424769 [Abstract] [Full Text] [Related]
35. Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts). Salido EC, Li XM, Yen PH, Martin N, Mohandas TK, Shapiro LJ. Nat Genet; 1996 May 30; 13(1):83-6. PubMed ID: 8673109 [Abstract] [Full Text] [Related]
36. Steroid sulfatase gene in XX males. Mohandas TK, Stern HJ, Meeker CA, Passage MB, Müller U, Page DC, Yen PH, Shapiro LJ. Am J Hum Genet; 1990 Feb 30; 46(2):369-76. PubMed ID: 2301402 [Abstract] [Full Text] [Related]
37. Localization of Y chromosome sequences and X chromosomal replication studies in XX males. Schempp W, Müller G, Scherer G, Bohlander SK, Rommerskirch W, Fraccaro M, Wolf U. Hum Genet; 1989 Jan 30; 81(2):144-8. PubMed ID: 2912884 [Abstract] [Full Text] [Related]
38. An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry. Schnur RE, Trask BJ, van den Engh G, Punnett HH, Kistenmacher M, Tomeo MA, Naids RE, Nussbaum RL. Am J Hum Genet; 1989 Nov 30; 45(5):706-20. PubMed ID: 2573275 [Abstract] [Full Text] [Related]
39. The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolution. Yen PH, Marsh B, Allen E, Tsai SP, Ellison J, Connolly L, Neiswanger K, Shapiro LJ. Cell; 1988 Dec 23; 55(6):1123-35. PubMed ID: 3203382 [Abstract] [Full Text] [Related]
40. 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 Dec 23; 12(1):36-9. PubMed ID: 9101220 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]