Williams-Beuren Syndrome: A Case Report
Williams syndrome is a rare neurodevelopmental disorder caused by the spontaneous deletion of genetic material from the region q11.23 of one member of the pair of chromosome 7, so that the person is hemizygous for those genes. Syndrome is a rarely genetic multisystem disorder that occurs equally in...
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| Main Authors: | , , |
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| Format: | Book |
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Cumhuriyet University,
2019-12-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |