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Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma by
- Hunt, D. M
- Armstrong, D. K. B
- Arnemann, J
- Buxton, R. S
- Dopping-Hepenstal, P. J. C
- Eady, R. A
- Hennies, H. C
- Hughes, A. E
- Kelsell, D. P
- Kuster, W
- Leigh, I. M
- McGrath, J. A
- Rickman, L
- Simrak, D
- Stevens, H. P
- Whittock, N. V
Material type: Text; Format:
print ; Literary form:
Not fiction
In: European Journal of Human Genetics 9 (3), 197-203.
Availability: Items available for loan: Staff publications (1)Call number: XX(11098.1).
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