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Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss-of-function mutation in CSTA. [electronic resource] by
- Moosbrugger-Martinz, V
- Jalili, A
- Schossig, A S
- Jahn-Bassler, K
- Zschocke, J
- Schmuth, M
- Stingl, G
- Eckl, K M
- Hennies, H C
- Gruber, R
Producer: 20160307
In:
The British journal of dermatology vol. 172
Availability: No items available.
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Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations. [electronic resource] by
- Gruber, R
- Rainer, G
- Weiss, A
- Udvardi, A
- Thiele, H
- Eckl, K M
- Schupart, R
- Nürnberg, P
- Zschocke, J
- Schmuth, M
- Volc-Platzer, B
- Hennies, H C
Producer: 20171024
In:
The British journal of dermatology vol. 176
Availability: No items available.
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