Evaluating the clinical utility of a long-read sequencing-based approach in genetic testing of fragile-X syndrome
Autor: | Hou, Fei, Mao, Aiping, Shan, Shan, Li, Yan, Meng, Wanli, Zhan, Jiahan, Nie, Wenying, Jin, Hua |
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Zdroj: | In Clinica Chimica Acta 1 November 2023 551 |
Databáze: | ScienceDirect |
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