Waardinburg syndrome - inherited deafness with pigmentary involvement
The Waardenburg syndrome was first clearly defined in 1951. The major clinical importance lies in the fact that about 20% of affected individuals are deaf. Furthermore, because the condition is inherited autosomal dominantly, there is a risk of the disorder being handed down from generation to gener...
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Main Author: | M.F. Macrae (Author) |
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Format: | Book |
Published: |
AOSIS,
1979-09-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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