新生儿遗传代谢性疾病筛查的进展与挑战

罗小平, 金圣娟

中国儿童保健杂志 ›› 2015, Vol. 23 ›› Issue (5) : 449-450.

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PDF(356 KB)
中国儿童保健杂志 ›› 2015, Vol. 23 ›› Issue (5) : 449-450. DOI: 10.11852/zgetbjzz2015-23-05-01
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新生儿遗传代谢性疾病筛查的进展与挑战

  • 罗小平, 金圣娟
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罗小平, 金圣娟. 新生儿遗传代谢性疾病筛查的进展与挑战[J]. 中国儿童保健杂志. 2015, 23(5): 449-450 https://doi.org/10.11852/zgetbjzz2015-23-05-01
中图分类号: R725.8   

参考文献

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[2] Bonham JR.Expanded newborn screening-progress into practice[J].Clinical Biochemistry, 2014, 47(9):697-698.
[3] Bennett MJ.Newborn screening for metabolic diseases: saving children's lives and improving outcomes[J].Clinical Biochemistry, 2014, 47(9):693-694.
[4] Rashed MS, Rahbeeni Z, Ozand PT.Application of electrospray tandem mass spectrometry to neonatal screening[J].Seminar Perinatology, 1999, 23:183-193.
[5] Cao Y, Yuan P, Wang YP, et al.The profile of newborn screening coverage in China[J].Journal of Medical Screening, 2009, 16(4):163-166.
[6] Mak CM, Lee HC, Chan AY, et al.Inborn errors of metabolism and expanded newborn screening: review and update[J].Critical Reviews in Clinical Laboratory Sciences, 2013, 50(6):142-162.
[7] Boyle CA, Bocchini JA Jr, Kelly J.Reflections on 50 years of newborn screening[J].Pediatrics, 2014, 133(6):961-963.

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