Epidermolysis bullosa simplex and mottled pigmentation: A new dominant syndrome-Reference-Cited by-同舟云学术

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Epidermolysis bullosa simplex and mottled pigmentation: A new dominant syndrome

Published:2008-04-23 Issue:3 Volume:15 Page:228-238
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Fischer T.,Gedde-Dahl T.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1979.tb00972.x/fullpdf

Reference23 articles.

1. Recurrent bullous eruption of the feet;Cockayne;Brit. J. Derm.,1938

2. Dyskeratosis congenita;Costello;Arch. Derm. (Chic.),1956

3. A case of epidermolysis bullosa. Transactions of the New York Der-matological Society, 22 October 1895;Elliot;J. cut. genit. urin. Dis.,1896

4. Universal dyschromatosis;Findlay;Brit. J. Derm.,1971

5. Dyskeratosis congenita with pigmentation, dystrophia unguium and leucoplakia oris;Garb;Arch. Derm. (Chic.),1944

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2. Exon 8 deletion of KRT5 in epidermolysis bullosa simplex with mottled pigmentation: A case report;The Journal of Dermatology;2023-09-02

3. Assessment of melanin distribution in epidermolysis bullosa simplex with mottled pigmentation: A case report;The Journal of Dermatology;2021-12-06

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