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Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation.
Hovnanian A, Rochat A, Bodemer C, Petit E, Rivers CA, Prost C, Fraitag S, Christiano AM, Uitto J, Lathrop M, Barrandon Y, de Prost Y. Hovnanian A, et al. Among authors: fraitag s. Am J Hum Genet. 1997 Sep;61(3):599-610. doi: 10.1086/515495. Am J Hum Genet. 1997. PMID: 9326325 Free PMC article.
[Cutaneous lesions in the orofaciodigital syndrome].
Habib K, Fraitag S, Couly G, de Prost Y. Habib K, et al. Among authors: fraitag s. Ann Pediatr (Paris). 1992 Sep;39(7):449-52. Ann Pediatr (Paris). 1992. PMID: 1416667 Portuguese.
[Dermatomyofibroma: a case in a child].
Fraitag S, Teillac-Hamel D, de Prost Y, Brousse N. Fraitag S, et al. Ann Dermatol Venereol. 1993;120(11):818-20. Ann Dermatol Venereol. 1993. PMID: 8210130 French. No abstract available.
349 results