Results of neonatal screening for congenital hypothyroidism and hyperphenylalaninemia in Zhejiang province from 1999 to 2022-Reference-Cited by-同舟云学术

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

Published:2023-12-01 Issue:6 Volume:52 Page:683-692
ISSN:1008-9292
Container-title:Journal of Zhejiang University (Medical Sciences)
language:en
Short-container-title:J Zhejiang Univ (Med Sci)

Author:

ZHOU Duo,YANG Rulai,HUANG Xinwen

Publisher

China Science Publishing & Media Ltd.

Subject

General Medicine

Link

https://engine.scichina.com/doi/pdf/CA5CF4A0E21F4F24A67E31A8950C6FB6

Reference33 articles.

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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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