American Academy of Pediatrics Committee on Genetics: New issues in newborn screening for phenylketonuria and congenital hypothyroidism. - Suppr | 超能文献

American Academy of Pediatrics Committee on Genetics: New issues in newborn screening for phenylketonuria and congenital hypothyroidism.

出版信息

Pediatrics. 1982 Jan;69(1):104-6.

Abstract

摘要

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引用本文的文献

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Screening of the newborn for hypothyroidism.

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Fifteen-year experience with screening for phenylketonuria with an automated fluorometric method.采用自动荧光法筛查苯丙酮尿症的十五年经验。

Am J Hum Genet. 1982 Sep;34(5):743-52.

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Phenylketonuria (PKU) and the single gene: an old story retold.苯丙酮尿症（PKU）与单基因：一个被重新讲述的古老故事。

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Finnish national screening for hypothyroidism. Few false positives, early therapy.芬兰全国甲状腺功能减退症筛查。假阳性少，治疗及时。

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J Inherit Metab Dis. 1989;12 Suppl 1:55-63. doi: 10.1007/BF01799286.