Author:
Van Neste D.,Degreef H.,Van Haute N.,Van Hee J.,Vandermaesen J.,Taieb A.,Maleville A.,Fontan D.,Bakry N.,Gillespie J. M.,Marshall R. C.
Reference11 articles.
1. Brown AC, Belser RB, Crounse RG, Wehr RF. A congenital hair defect: trichoschisis with alternating birefringence and low sulfur content. J Invest Dermatol, 54, 496–509, 1970
2. Pollitt RJ, Stonier PD. Proteins of normal hair and of cystine-deficient hair from mentally retarded siblings. Biochem J, 122, 433–444, 1971
3. Gold RJM, Kachra Z. Molecular defect in hydrotic ectodermal dysplasia. In Proceedings of the First Human Hair Symposium, Atlanta, 1973 (Brown AC, ed), pp. 260–276. New York: Medcom, 1974
4. Price VH, Odom RB, Ward WH, Jones FT. Trichothiodystrophy: sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complex. Arch Dermatol, 116, 1375–1384, 1980
5. Van Neste D, Boré P. Trichothiodystrophie: une étude morphologique et biochimique Ann Dermatol Vénéréol, 110, 409–417, 1983
Cited by
6 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献