Results of neonatal screening for congenital hypothyroidism and hyperphenylalaninemia in Zhejiang province from 1999 to 2022

Author:

ZHOU Duo,YANG Rulai,HUANG Xinwen

Publisher

China Science Publishing & Media Ltd.

Subject

General Medicine

Reference33 articles.

1. ZHAO Zhengyan, GU Xuefan. Newborn screening for genetic metabolic diseases (2nd Edition)[M]. Beijing: People’s Medical Publishing House, 2015: 10. (in Chinese)..

2. 赵正言, 顾学范. 新生儿遗传代谢病筛查(第2版)[M]. 北京: 人民卫生出版社, 2015: 10..

3. LI Qiang, ZHOU Ying, XU Yanhua, et al. Analysis on neonatal screening for inherited metabolic diseases in Zhejiang Province from 1999 to 2018[J]. China Preventive Medicine Journal, 2019, 31(11): 1081-1085. (in Chinese).

4. 李强, 周莹, 徐艳华, 等. 1999—2018年浙江省新生儿遗传代谢病筛查情况分析[J]. 预防医学, 2019, 31(11): 1081-1085..

5. LAI Ting, LI Xiaohong, DENG Kui, et al. Analysis on neonatal screening coverage rate in China from 2006 to 2016[J]. Maternal and Child Health Care in China, 2018, 33(16): 3601-3604. (in Chinese)..

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