Identifying of 22q11.2 variations in Chinese patients with development delay
Abstract Background 22q11.2 variation is a significant genetic factor relating to development delay and/or intellectual disability. However, the prevalence, genetic characteristics and clinical phenotype in Chinese patients are unknown. Methods In total 6034 patients with development delay and/or in...
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| Main Authors: | , , , , |
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| Format: | Book |
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BMC,
2021-01-01T00:00:00Z.
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