The dental phenotype of primary dentition in SATB2-associated syndrome: a report of three cases and literature review
Abstract Background SATB2-associated syndrome (SAS; OMIM: 612,313) is an autosomal dominant inherited multisystemic disorder caused by several variants of the SATB2 gene. SAS is characterized by intellectual disability, developmental delay, severe speech anomalies, craniofacial anomalies, and dental...
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| Main Authors: | , , |
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| Format: | Book |
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BMC,
2022-11-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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