Results 111 to 120 of about 1,774 (212)

Epidermolysis bullosa dystrophica, hypoplastic type, associated with Pelger-Huet anomaly. [PDF]

open access: bronze, 1967
I. Cat   +6 more
openalex   +1 more source

Ophthalmic phenotype associated with a novel mutation in <i>LAMB3</i> gene linked to uncommon Intermediate Junctional Epidermolysis Bullosa. [PDF]

open access: yesAm J Ophthalmol Case Rep
Alzaben KA   +5 more
europepmc   +1 more source

Dystrophia unguium mediana canaliformis Heller. [PDF]

open access: yes, 1974
Putz, Reinhard   +2 more
core   +1 more source

Oral manifestations of epidermolysis bullosa dystrophica: a rare genetic disease. [PDF]

open access: yesBMJ Case Rep, 2013
Parushetti AD   +3 more
europepmc   +1 more source

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