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Journal Abstract Search

189 related items for PubMed ID: 2659403

  • 1. [The genetics and molecular genetics of X-chromosomal recessive ichthyosis].
    Herrmann FH.
    Dermatol Monatsschr; 1989; 175(4):197-202. PubMed ID: 2659403
    [Abstract] [Full Text] [Related]

  • 2. [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. PubMed ID: 3468016
    [No Abstract] [Full Text] [Related]

  • 3. [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. PubMed ID: 3470217
    [No Abstract] [Full Text] [Related]

  • 4. [Ophthalmologic findings in X chromosomal recessive ichthyosis].
    Voss M, Jünemann R.
    Dermatol Monatsschr; 1986; 172(4):209-11. PubMed ID: 3721026
    [No Abstract] [Full Text] [Related]

  • 5. Linkage studies in a family with X-linked recessive ichthyosis employing a cloned DNA sequence from the distal short arm of the X chromosome.
    Wieacker P, Davies KE, Mevorah B, Ropers HH.
    Hum Genet; 1983; 63(2):113-6. PubMed ID: 6301973
    [Abstract] [Full Text] [Related]

  • 6. [Biochemical diagnosis of X chromosomal ichthyosis].
    Meyer JC, Gilardi S.
    Hautarzt; 1986 Apr; 37(4):205-9. PubMed ID: 3457782
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 41(2):184-7. PubMed ID: 1785631
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  • 14. [Prenatal diagnosis of X chromosome recessive ichthyosis in uncultured chorion cells].
    Grimm U, Herrmann FH, Machill G, Knoll W, Schütz M.
    Dermatol Monatsschr; 1988 Nov 01; 174(2):103-5. PubMed ID: 3131162
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  • 16. [Recurrent corneal erosion in epidermolysis bullosa simplex Köbner and X-chromosomal ichthyosis].
    Steuhl KP, Anton-Lamprecht I, Arnold ML, Thiel HJ.
    Fortschr Ophthalmol; 1988 Nov 01; 85(6):669-71. PubMed ID: 3220383
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  • 17. Steroid sulphatase deficiency in patients initially diagnosed as ichthyosis vulgaris or recessive X-linked ichthyosis.
    Yoshiike T, Matsui T, Ogawa H.
    Br J Dermatol; 1985 Apr 01; 112(4):431-3. PubMed ID: 3857937
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  • 18. Steroid sulfatase deficiency and the genetics of the short arm of the human X chromosome.
    Shapiro LJ.
    Adv Hum Genet; 1985 Apr 01; 14():331-81, 388-9. PubMed ID: 2859745
    [No Abstract] [Full Text] [Related]

  • 19. Carrier identification in steroid sulphatase deficiency and recessive X-linked ichthyosis.
    Lykkesfeldt G, Lykkesfeldt AE.
    Acta Derm Venereol; 1986 Apr 01; 66(2):134-8. PubMed ID: 2424236
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  • 20. Autosomal dominant ichthyosis and X-linked ichthyosis. Comparison of their clinical and histological phenotypes.
    Mevorah B, Krayenbuhl A, Bovey EH, van Melle GD.
    Acta Derm Venereol; 1991 Apr 01; 71(5):431-4. PubMed ID: 1684474
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