Prenatal phenotype features and genetic etiology of the Williams-Beuren syndrome and literature review
ObjectiveTo share our experience on prenatal diagnosis of Williams-Beuren syndrome(WBS) and to improve the awareness, diagnosis, and intrauterine monitoring of the fetuses of this disease.MethodsThe study retrospectively evaluated 14 cases of WBS diagnosed prenatally by single nucleotide polymorphis...
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Main Authors: | , , , , , , , , |
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Format: | Book |
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Frontiers Media S.A.,
2023-03-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
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A1234.567 |
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Copy 1 | Available |