Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome
Abstract Background Prader-Willi syndrome (PWS) is a complex disorder caused by impaired paternally expressed genes on chromosome 15q11-q13. Variable findings have been reported about the phenotypic differences among PWS genetic subtypes. Methods A total of 110 PWS patients were diagnosed from 8,572...
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Main Authors: | , , , , , , , , |
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Format: | Book |
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BMC,
2022-07-01T00:00:00Z.
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A1234.567 |
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