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4. Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias. Itin PH; Pittelkow MR J Am Acad Dermatol; 1990 May; 22(5 Pt 1):705-17. PubMed ID: 2189905 [TBL] [Abstract][Full Text] [Related]
5. Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity. Stefanini M; Lagomarsini P; Arlett CF; Marinoni S; Borrone C; Crovato F; Trevisan G; Cordone G; Nuzzo F Hum Genet; 1986 Oct; 74(2):107-12. PubMed ID: 3770739 [TBL] [Abstract][Full Text] [Related]
11. [Congenital hair dysplasia: management and value of various diagnostic methods]. Van Neste D Ann Dermatol Venereol; 1989; 116(3):251-63. PubMed ID: 2742306 [No Abstract] [Full Text] [Related]
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14. Prenatal diagnosis in a subset of trichothiodystrophy patients defective in DNA repair. Sarasin A; Blanchet-Bardon C; Renault G; Lehmann A; Arlett C; Dumez Y Br J Dermatol; 1992 Nov; 127(5):485-91. PubMed ID: 1281671 [TBL] [Abstract][Full Text] [Related]
16. Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity. Stefanini M; Lagomarsini P; Giorgi R; Nuzzo F Mutat Res; 1987 Jun; 191(2):117-9. PubMed ID: 3600693 [TBL] [Abstract][Full Text] [Related]