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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Elsevier,
2024-09-01T00:00:00Z.
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A1234.567 |
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| Kopie 1 | Beschikbaar |