CLINICAL CASE OF CHROMOSOME 22Q11.2 DELETION SYNDROME (DI-GEORGIE SYNDROME)
A clinical case of orphan genetic pathology - Di Georgi syndrome in a child in the neonatal period is presented. The complexity of timely diagnosis of this complication is demonstrated.
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
The Publishing House Medicine and Enlightenment,
2020-02-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |