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Comparison of helix stability in wild-type and mutant LamB signal sequences.
Syntaxin 13, a genetic modifier of mutant CHMP2B in frontotemporal dementia, is required for autophagosome maturation.
Colobinae
Functional improvement after patients with rheumatoid arthritis start a new disease modifying antirheumatic drug (DMARD) associated with frequent changes in DMARD: the CORRONA database.
Denuded congenital lesions: recessive dystrophic epidermolysis bullosa.
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Denuded congenital lesions: recessive dystrophic epidermolysis bullosa.
Fleming KF, Wu JJ, Dyson SW, Dadras SS, Metz BJ. Denuded congenital lesions: recessive dystrophic epidermolysis bullosa. Dermatol Online J. 2009 Apr 15; 15(4):4.
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PubMed
subject areas
Abnormalities, Multiple
Collagen Type VII
Epidermolysis Bullosa Dystrophica
Female
Genes, Recessive
Humans
Hypertelorism
Infant, Newborn
Keratinocytes
Microscopy, Electron
Palate
Retrognathia
authors with profiles
Soheil Sadr Dadras MD, PhD