Medicine
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22 january 2021 17:37:18 |
| Identifying of 22q11.2 variations in Chinese patients with development delay (BMC Medical Genomics) |
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Tweet 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 u... |
| 176 viewsCategory: Genomics, Medicine |
 Correlation analysis of IL-11 polymorphisms and Hirschsprung disease subtype susceptibility in Southern Chinese Children (BMC Medical Genomics)Expression and gene regulatory network of SNHG1 in hepatocellular carcinoma (BMC Medical Genomics) 
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