Statistics for Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome
Total visits
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| Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome | 177 |
Total visits per month
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| December 2024 | 0 |
| January 2025 | 0 |
| February 2025 | 0 |
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| April 2025 | 0 |
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File Visits
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| 13073_2019_Article_630.pdf | 128 |
| java.util.UUID:fe767fc3-109f-4f22-b0fc-49763ce7a759 | 41 |
| java.util.UUID:57edb8ad-2e0c-49eb-9605-bd5a6895d11e | 19 |
| java.util.UUID:c7bdadc0-6866-4965-a938-5b3bfd891de9 | 9 |
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