209 related articles for article (PubMed ID: 3169744)
1. Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency).
Wirth B; Herrmann FH; Neugebauer M; Gillard EF; Wulff K; Stein C; von Figura K; Ferguson-Smith MA; Gal A
Hum Genet; 1988 Oct; 80(2):191-2. PubMed ID: 3169744
[TBL] [Abstract][Full Text] [Related]
2. Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers.
Yates JR; Goudie DR; Gillard EF; Aitken DA; Affara NA; Clayton JF; Tippett PA; Ferguson-Smith MA
Genomics; 1987 Sep; 1(1):52-9. PubMed ID: 3478297
[TBL] [Abstract][Full Text] [Related]
3. Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels.
Ballabio A; Carrozzo R; Parenti G; Gil A; Zollo M; Persico MG; Gillard E; Affara N; Yates J; Ferguson-Smith MA
Genomics; 1989 Jan; 4(1):36-40. PubMed ID: 2644167
[TBL] [Abstract][Full Text] [Related]
4. Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency).
Gillard EF; Affara NA; Yates JR; Goudie DR; Lambert J; Aitken DA; Ferguson-Smith MA
Nucleic Acids Res; 1987 May; 15(10):3977-85. PubMed ID: 2884621
[TBL] [Abstract][Full Text] [Related]
5. X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome.
Ballabio A; Parenti G; Tippett P; Mondello C; Di Maio S; Tenore A; Andria G
Hum Genet; 1986 Mar; 72(3):237-40. PubMed ID: 3007328
[TBL] [Abstract][Full Text] [Related]
6. Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome.
Ballabio A; Sebastio G; Carrozzo R; Parenti G; Piccirillo A; Persico MG; Andria G
Hum Genet; 1987 Dec; 77(4):338-41. PubMed ID: 3480263
[TBL] [Abstract][Full Text] [Related]
7. Two cases of steroid sulfatase deficiency with complex phenotype due to contiguous gene deletions.
Nishimura S; Masuda H; Matsumoto T; Sakura N; Matsumoto T; Ueda K
Am J Med Genet; 1991 Sep; 40(3):260-3. PubMed ID: 1951426
[TBL] [Abstract][Full Text] [Related]
8. X chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis).
Cooke A; Gillard EF; Yates JR; Mitchell MJ; Aitken DA; Weir DM; Affara NA; Ferguson-Smith MA
Hum Genet; 1988 May; 79(1):49-52. PubMed ID: 3163320
[TBL] [Abstract][Full Text] [Related]
9. Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223.
Tiepolo L; Zuffardi O; Fraccaro M; di Natale D; Gargantini L; Müller CR; Ropers HH
Hum Genet; 1980; 54(2):205-6. PubMed ID: 6930361
[TBL] [Abstract][Full Text] [Related]
10. [Microsomal sulfatase deficiency in X chromosome-linked ichthyosis].
Meyer JC; Schnyder UW
Hautarzt; 1982 Feb; 33(2):82-8. PubMed ID: 6951821
[TBL] [Abstract][Full Text] [Related]
11. Gene diagnosis in X-linked ichthyosis.
Herrmann FH; Wirth B; Wulff K; Hadlich J; Voss M; Gillard EF; Kruse TA; Ferguson-Smith MA; Gal A
Arch Dermatol Res; 1989; 280(8):457-61. PubMed ID: 2493225
[TBL] [Abstract][Full Text] [Related]
12. Steroid sulfatase deficiency and the genetics of the short arm of the human X chromosome.
Shapiro LJ
Adv Hum Genet; 1985; 14():331-81, 388-9. PubMed ID: 2859745
[No Abstract] [Full Text] [Related]
13. A new syndrome of anosmia, ichthyosis, hypogonadism, and various neurological manifestations with deficiency of steroid sulfatase and arylsulfatase C.
Sunohara N; Sakuragawa N; Satoyoshi E; Tanae A; Shapiro LJ
Ann Neurol; 1986 Feb; 19(2):174-81. PubMed ID: 3516063
[TBL] [Abstract][Full Text] [Related]
14. [The enzyme arylsulfatase C and steroid sulfatase as biochemical markers and pathogenetic factors in X-chromosome recessively inherited ichthyosis].
Schlenzka K
Dermatol Monatsschr; 1983; 169(10):621-4. PubMed ID: 6580240
[No Abstract] [Full Text] [Related]
15. Steroid sulfatase deficiency and X-linked ichthyosis.
Shapiro LJ
Clin Biochem; 1979 Dec; 12(6):205. PubMed ID: 294955
[No Abstract] [Full Text] [Related]
16. X-linked ichthyosis and X-linked placental sulfatase deficiency: a disease entity. Histochemical observations.
Jöbsis AC; De Groot WP; Tigges AJ; De Bruijn HW; Rijken Y; Meijer AE; Marinkovic-Ilsen A
Am J Pathol; 1980 May; 99(2):279-89. PubMed ID: 6929654
[TBL] [Abstract][Full Text] [Related]
17. Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency.
Ballabio A; Parenti G; Napolitano E; Di Natale P; Andria G
Hum Genet; 1985; 70(4):315-7. PubMed ID: 3860470
[TBL] [Abstract][Full Text] [Related]
18. 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; 84(13):4519-23. PubMed ID: 3474618
[TBL] [Abstract][Full Text] [Related]
19. Rapid laboratory diagnostic of X-linked ichthyosis.
Meyer JC; Groh V; Giger V; Weiss H; Varbelow H; Schnyder UW
Dermatologica; 1982 Apr; 164(4):249-57. PubMed ID: 6953038
[TBL] [Abstract][Full Text] [Related]
20. Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiency.
Ballabio A; Zollo M; Carrozzo R; Caiulo A; Zuffardi O; Cascioli CF; Viggiano D; Strisciuglio P
Am J Med Genet; 1991 Nov; 41(2):184-7. PubMed ID: 1785631
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]