Chromosome and blood marker studies in families of patients affected by xeroderma pigmentosum and trichothiodystrophy
- 1 July 1988
- journal article
- research article
- Published by Elsevier BV in Mutation Research Letters
- Vol. 208 (3-4), 159-161
- https://doi.org/10.1016/0165-7992(88)90053-x
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivityMutation Research Letters, 1987
- Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivityHuman Genetics, 1986
- Trichothiodystrophy: an ultrastructural study of the hair follicleBritish Journal of Dermatology, 1985
- PIBIDS: Tay's syndrome and xeroderma pigmentosumJournal of the American Academy of Dermatology, 1985
- Trichothiodystrophy: sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complexArchives of Dermatology, 1980