Application of next generation sequencing in the screening of monogenic diseases in China,2021:a consensus among Chinese newborn screening experts
被引量:9
摘要
Newborn screening(NBS)refers to a maternal and newborn healthcare technology,in which special examinations of congenital and genetic diseases that could seriously impact the health of newborns,are implemented during the neonatal period to provide early diagnosis and treatment[1].With a history of more than 60 years,NBS has advanced greatly due to technological progress resulting in significant improvement in the number of diseases covered by NBS and in screening efficiency[2-7].
参考文献2
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1中华预防医学会出生缺陷与控制专业委员会新生儿遗传代谢病筛查学组,中华医学会儿科学分会新生儿学组,赵正言,周文浩,童凡,王剑,肖锐.中国新生儿基因筛查专家共识:高通量测序在单基因病筛查中的应用[J].中华实用儿科临床杂志,2023,38(1):31-36. 被引量:4
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6张伟然,赵正言.新生儿疾病基因筛查研究进展[J].中华儿科杂志,2020,58(12):1033-1037. 被引量:13
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7Jia-Jia Chen,Bing-Yan Cao,Chang Su,Min Liu,Di Wu,Wen-Jing Li,Chun-Xiu Gong.A Chinese girl with Turner syndrome and Duchenne muscular dystrophy: diagnosis and management of this "dual diagnosis"[J].Chinese Medical Journal,2021(6):743-745.
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9郑金仙,韩帅,叶文,姚树列,祁鸣,陈建芬,徐红.基于孕前优生平台的育龄女性假肥大型肌营养不良症携带者筛查模式[J].中华医学遗传学杂志,2021,38(5):485-487. 被引量:1
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同被引文献50
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1中华预防医学会出生缺陷与控制专业委员会新生儿遗传代谢病筛查学组,中华医学会儿科学分会新生儿学组,赵正言,周文浩,童凡,王剑,肖锐.中国新生儿基因筛查专家共识:高通量测序在单基因病筛查中的应用[J].中华实用儿科临床杂志,2023,38(1):31-36. 被引量:4
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2唐东江,马燮琴,宋诚燕,林本蘅,吴淑祯,蒋思慧,萧广仁.干血纸片法用于广东人G6PD基因点突变筛查研究[J].中华血液学杂志,1998,19(4):189-191. 被引量:17
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3瞿宇晋,都娟,李尔珍,杨艳玲,邹丽萍,白晋丽,王红,金煜炜,宋昉.脊髓性肌萎缩症的SMN1基因点突变分析[J].中华医学遗传学杂志,2011,28(2):121-126. 被引量:6
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引证文献9
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2黄喆兰(综述),周文浩(审校).儿童脑白质营养不良的临床遗传学研究进展[J].中国当代儿科杂志,2022,24(6):711-716.
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3杨茹莱,沈亚平,陈迟,周莹,徐艳华,舒强.2009-2021年浙江省新生儿遗传代谢病基因型分析[J].预防医学,2022,34(8):760-764. 被引量:5
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二级引证文献15
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3中华预防医学会出生缺陷预防与控制专业委员会新生儿遗传代谢病筛查学组,顾学范,赵正言,杨茹莱,朱军,王华,文伟,虞斌.新生儿遗传代谢病筛查组织管理及血片采集技术规范专家共识[J].中华新生儿科杂志(中英文),2023,38(6):321-326. 被引量:6
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