Clinical and genetic analysis of two phenotypically normal families carrying 4p16.1 microduplications
Objective: To help determine the pathogenicity of 4p16.1 microduplications, we reported two asymptomatic families carrying this variation. Case report: We present the prenatal diagnosis and genetic analysis of two normal families with 4p16.1 microduplications. Conclusion: This paper highlights two f...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Elsevier,
2024-09-01T00:00:00Z.
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| 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 |