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Items: 1 to 20 of 130

1.

Heterozygote detection in steroid sulphatase deficiency.

Müller CR, Migl B, Ropers HH, Happle R.

Lancet. 1980 Mar 8;1(8167):546-7. No abstract available.

PMID:
6102271
2.

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.

PMID:
3860470
3.

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.

PMID:
6930361
4.

X-linked ichthyosis due to steroid sulfatase deficiency associated with hypogonadism and anosmia.

Andria G, Ballabio A, Parenti G.

Ann Neurol. 1987 Jul;22(1):98-9. No abstract available.

PMID:
3477126
5.

Carrier identification in steroid sulphatase deficiency and recessive X-linked ichthyosis.

Lykkesfeldt G, Lykkesfeldt AE.

Acta Derm Venereol. 1986;66(2):134-8.

PMID:
2424236
6.

[Arylsulfatase C deficiency in leukocytes in patients and carrier of X-chromosome recessive ichthyosis].

Hadlich J, Herrmann FH, Grimm U.

Dermatol Monatsschr. 1986;172(10):624-6. German. No abstract available.

PMID:
3468016
7.

[X-chromosomal recessive ichthyosis. Detection of heterozygote status in genetically possible carriers by determination of arylsulfatase C activity].

Hadlich J, Herrmann FH, Grimm U.

Dermatol Monatsschr. 1986;172(12):734-6. German. No abstract available.

PMID:
3470217
8.

Review: genetics of steroid sulphatase deficiency and X-linked ichthyosis.

Crawfurd MA.

J Inherit Metab Dis. 1982;5(3):153-63. Review.

PMID:
6820437
9.

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.

PMID:
3480263
10.

Steroid sulfatase deficiency and X-linked ichthyosis.

Shapiro LJ.

Clin Biochem. 1979 Dec;12(6):205. No abstract available.

PMID:
294955
11.

Further evidence for the assignment of the steroid sulfatase X-linked ichthyosis locus to the telomer of Xp.

Müller CR, Wahlström J, Ropers HH.

Hum Genet. 1981;58(4):446. No abstract available.

PMID:
6948769
12.

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.

PMID:
3163320
13.

Steroid sulphatase deficiency associated with testis cancer.

Lykkesfeldt G, Høyer H, Lykkesfeldt AE, Skakkebaek NE.

Lancet. 1983 Dec 24-31;2(8365-66):1456.

PMID:
6140547
14.
15.
16.

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, et al.

Proc Natl Acad Sci U S A. 1987 Jul;84(13):4519-23.

17.
18.

Partial lyonisation of steroid sulphatase gene in single hair roots.

Willems PJ, de Bruijn HW, Groenhuis A, Mooyaart BR, Berger R.

J Inherit Metab Dis. 1986;9(2):156-62.

PMID:
3091922
19.

More on X-linked ichthyosis, steroid sulfatase deficiency, and hypogonadism and anosmia.

Andria G, Ballabio A, Parenti G.

Ann Neurol. 1988 Jan;23(1):103. No abstract available.

PMID:
3422798
20.

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.

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