Results 161 to 163 of about 2,415 (163)

Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families

Frontiers in Medicine
exaly  

Epidermolysis bullosa tarda simplex.

Dermatologica, 2010
openaire   +1 more source

Epidermolysis bullosa simplex in Slovenia:

2003
Dragoš, Vlasta, Kansky, Aleksej, Komel, Radovan, Liović, Mirjana, Podrumac, Božena   +4 more
openaire   +1 more source