Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
复制标题
因 21-羟化酶缺乏所致的典型先天性肾上腺增生新生儿筛查的全球经验。
作者：
S. Pang;M. Wallace;L. Hofman;H. Thuline;C. Dorche;I. Lyon;Robert H. Dobbins;S. Kling;K. Fujieda;S. Suwa
