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43. Heritable fragile sites on human chromosomes. VI. Characterization of the fragile site at 12q13. Sutherland GR; Hinton L Hum Genet; 1981; 57(2):217-9. PubMed ID: 7194847 [No Abstract] [Full Text] [Related]
44. [Incidence of hereditary dystrophic bullous epidermolysis and progressive muscular dystrophy in one family]. de Weerdt CJ; Castelein S Ned Tijdschr Geneeskd; 1972 Jul; 116(30):1264-8. PubMed ID: 5041295 [No Abstract] [Full Text] [Related]
46. A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex. Hovnanian A; Pollack E; Hilal L; Rochat A; Prost C; Barrandon Y; Goossens M Nat Genet; 1993 Apr; 3(4):327-32. PubMed ID: 7526933 [TBL] [Abstract][Full Text] [Related]
47. Multiple osteochondroses of the feet in a West Indian family. Brown ID; Shaw DG J Bone Joint Surg Br; 1973 Nov; 55(4):864-70. PubMed ID: 4766194 [No Abstract] [Full Text] [Related]
48. [Incidence of structural disorders of teeth in hereditary epidermolysis bullosa]. Gábris K; Csiba A; Orosz M Fogorv Sz; 1996 Jan; 89(1):7-10. PubMed ID: 8713615 [TBL] [Abstract][Full Text] [Related]
49. Epidermolysis bullosa in Finland. Clinical features, morphology and relation to collagen metabolism. Kero M Acta Derm Venereol Suppl (Stockh); 1984; 110():1-51. PubMed ID: 6331034 [TBL] [Abstract][Full Text] [Related]
54. [Hereditary epidermolysis bullosa]. Jovanic M; Rasic D; Stojanovic D Bull Fed Soc Gynecol Obstet Lang Fr; 1968; 20(3):221-5. PubMed ID: 5713249 [No Abstract] [Full Text] [Related]
55. [Epidermolysis bullosa]. García Pérez A An R Acad Nac Med (Madr); 1999; 116(2):387-413; discussion 413-5. PubMed ID: 10682398 [TBL] [Abstract][Full Text] [Related]