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Results of search for 'au:"Fiebig, B S"'
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Authors
Aslanidis, C
Babilas, P
Fiebig, B S
Hansen, J
Kellner, S
Kellner, U
Landthaler, M
Renner, A B
Röcken, C
Schmitz, G
Schroeder, J
Vogt, T
Weber, B H
Weber, B H F
Weinitz, S
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Topics
Amyloidosis, Familial
Electroretinography
Evidence-Based Medicine
Female
Genetic Predisposition to Disease
Genetic Testing
Humans
Mutation, Missense
Oncostatin M Receptor beta Subunit
Pedigree
Retinal Degeneration
Retinoscopy
diagnosis
genetics
trends
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Languages
English
German
Your search returned 2 results.
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1.
[Evidence-based diagnostic approach to inherited retinal dystrophies 2009].
[electronic resource]
by
Kellner, U
Kellner, S
Renner, A B
Fiebig, B S
Weinitz, S
Weber, B H
Producer:
20100416
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 226
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2.
Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis.
[electronic resource]
by
Babilas, P
Fiebig, B S
Aslanidis, C
Hansen, J
Röcken, C
Schroeder, J
Schmitz, G
Weber, B H F
Landthaler, M
Vogt, T
Producer:
20100311
In:
The British journal of dermatology
vol. 161
Online resources:
Available from publisher's website
Availability:
No items available.
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