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2. [Dominant epidermolysis bullosa dystrophica of Cockayne-Touraine. Presentation of a familial case and cytogenetic investigation]. Amerio P; Pallotta R; Di Donato D; Dalprà L G Ital Dermatol Venereol; 1988 Sep; 123(9):417-20. PubMed ID: 3243581 [No Abstract] [Full Text] [Related]
3. [Cytogenetic studies on some rarer dermatoses]. Back F; Maestri D Hautarzt; 1966 Jan; 17(1):35-6. PubMed ID: 4963733 [No Abstract] [Full Text] [Related]
4. [Back mutation mosaic: a new genetic principle]. Happle R Hautarzt; 1997 Sep; 48(9):613-4. PubMed ID: 9410843 [No Abstract] [Full Text] [Related]
5. 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]
6. Some genetic aspects of dermatology: a review. Wells RS Clin Exp Dermatol; 1980 Mar; 5(1):1-11. PubMed ID: 6994956 [No Abstract] [Full Text] [Related]
8. [Apropos of 28 cases of epidermolysis bullosa in 11 families of which 1 family was studied from the genetic point of view without discovery of evidnece of linkage]. Huriez C; Deminatti ; Agache P; Faustin M Bull Soc Fr Dermatol Syphiligr; 1968; 75(6):750-5. PubMed ID: 5712981 [No Abstract] [Full Text] [Related]
9. Epidermolysis bullosa and the search for the basis of hereditary disorders of the skin. Epstein EH J Dermatol; 1992 Nov; 19(11):790-2. PubMed ID: 1293164 [TBL] [Abstract][Full Text] [Related]
10. Epidermolysis bullosa dystrophica dominans in two families in the Faroe Islands. A clinico-genetic study of 56 living individuals. Joensen HD Acta Derm Venereol; 1973; 53(1):53-60. PubMed ID: 4120809 [No Abstract] [Full Text] [Related]
12. [Hereditary bullous epidermolyses. Recent aspects of diagnosis and therapy]. Krieg T; Schurig V; Braun-Falco O Hautarzt; 1986 Apr; 37(4):185-9. PubMed ID: 3009355 [TBL] [Abstract][Full Text] [Related]
13. [Special aspects of anesthesia in patients with epidermolysis bullosa based on a case example]. Scherhag A; Dick W Anaesthesiol Reanim; 1998; 23(5):129-33. PubMed ID: 9854331 [TBL] [Abstract][Full Text] [Related]
15. What's new in pediatric dermatology?: part I. Diagnosis and pathogenesis. Pride HB; Tollefson M; Silverman R J Am Acad Dermatol; 2013 Jun; 68(6):885.e1-12; quiz 897-8. PubMed ID: 23680204 [TBL] [Abstract][Full Text] [Related]
16. Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals. Kiritsi D; Cosgarea I; Franzke CW; Schumann H; Oji V; Kohlhase J; Bruckner-Tuderman L; Has C J Invest Dermatol; 2010 Jun; 130(6):1741-6. PubMed ID: 20164844 [No Abstract] [Full Text] [Related]
17. [Monogenic inheritance: the skin]. Moser H Ther Umsch; 1986 Dec; 43(12):922-30. PubMed ID: 3824264 [No Abstract] [Full Text] [Related]