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Journal Abstract Search

284 related items for PubMed ID: 8205320

  • 1. Syndromes associated with trichothiodystrophy.
    Tolmie JL, de Berker D, Dawber R, Galloway C, Gregory DW, Lehmann AR, McClure J, Pollitt RJ, Stephenson JB.
    Clin Dysmorphol; 1994 Jan; 3(1):1-14. PubMed ID: 8205320
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  • 2. [Trichothiodystrophy: progresssive manifestations].
    Foulc P, Jumbou O, David A, Sarasin A, Stalder JF.
    Ann Dermatol Venereol; 1999 Oct; 126(10):703-7. PubMed ID: 10604009
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  • 3. [Trichothiodystrophy. Hair examination as a diagnostic tool].
    Hansen LK, Wulff K, Brandrup F.
    Ugeskr Laeger; 1993 Jun 21; 155(25):1949-52. PubMed ID: 8317059
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  • 4. Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.
    Itin PH, Sarasin A, Pittelkow MR.
    J Am Acad Dermatol; 2001 Jun 21; 44(6):891-920; quiz 921-4. PubMed ID: 11369901
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  • 5. [Trichothiodystrophy].
    Meynadier J, Guillot B, Barnéon G, Djian B, Lévy A.
    Ann Dermatol Venereol; 1987 Jun 21; 114(12):1529-36. PubMed ID: 3445983
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  • 6. [Trichothiodystrophy: a morphological and biochemical study].
    Van Neste D, Boré P.
    Ann Dermatol Venereol; 1983 Jun 21; 110(5):409-17. PubMed ID: 6625462
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  • 7. [Xeroderma pigmentosum and related syndromes].
    Berneburg M, Krutmann J.
    Hautarzt; 2003 Jan 21; 54(1):33-40. PubMed ID: 12567255
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  • 8. [Trichothiodystrophy: PIBIDS syndrome].
    Jiménez-Puya R, Moreno-Giménez JC, Camacho-Martínez F, Ferrando-Barbera J, Grimalt R.
    Actas Dermosifiliogr; 2007 Apr 21; 98(3):183-7. PubMed ID: 17504703
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  • 16. A temperature-sensitive disorder in basal transcription and DNA repair in humans.
    Vermeulen W, Rademakers S, Jaspers NG, Appeldoorn E, Raams A, Klein B, Kleijer WJ, Hansen LK, Hoeijmakers JH.
    Nat Genet; 2001 Mar 21; 27(3):299-303. PubMed ID: 11242112
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  • 18. Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias.
    Itin PH, Pittelkow MR.
    J Am Acad Dermatol; 1990 May 21; 22(5 Pt 1):705-17. PubMed ID: 2189905
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  • 19. Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings.
    Przedborski S, Ferster A, Goldman S, Wolter R, Song M, Tonnesen T, Pollitt RJ, Vamos E.
    Am J Med Genet; 1990 Apr 21; 35(4):566-73. PubMed ID: 2333887
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  • 20. Sabinas syndrome in monozygotic twins.
    López-García DR, Salas-Alanis JC, Christiano AM, Ocampo-Candiani J, Gómez-Flores M.
    Clin Exp Dermatol; 2009 Jul 21; 34(5):e94-8. PubMed ID: 19438561
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