Progress of newborn screening in China

Author:

JIANG Hongli,YANG Rulai,DONG Ao,WU Benqing,ZHAO Zhengyan

Publisher

China Science Publishing & Media Ltd.

Subject

General Medicine

Reference67 articles.

1. 赵正言, 顾学范. 新生儿遗传代谢病筛查[M]. 2版. 北京: 人民卫生出版社, 2015: 1-7..

2. ZHAO Zhengyan, GU Xuefan. Newborn genetic meta-bolic diseases screenig[M]. 2nd ed. Beijing: People’s Medical Publishing House, 2015: 1-7. (in Chinese).

3. GROSSE S D, DEZATEUX C. Newborn screening for inherited metabolic disease. Lancet, 2007, 369: 5-6.

4. GUTHRIE R, SUSI A. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants. Pediatrics, 1963, 32: 338-343.

5. DUSSAULT J H, LABERGE C. Thyroxine (T4) deter-mination by radioimmunological methods in dried blood dried blood eluate: new diagnostic method of neonatal hypothyroidism?[J]. Union Med Can, 1973, 102(10): 2062-2064..

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