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[会议论文] 作者：Yanyan Cao,Yujin Qu,Jinli Bai,Yuwei Jin,Hong Wang,Fang Song,
来源：2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份：2014
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[会议论文] 作者：JinLi Bai,YuJin Qu,YanYan Cao,Yan Li,WenHui Zhang,YuWei Jin,Hong Wang,Fang Song,
来源：2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份：2014
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[会议论文] 作者：JinLi Bai,YuJin Qu,YanYan Cao,Yan Li,WenHui Zhang,YuWei Jin,Hong Wang,Fang Song,
来源：2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份：2014
Background: Crigler-Najjar syndrome (CN-I) is a very rare autosomal recessive disease caused by the homozygous or compound heterozygous mutations of UPD-glucuronosyl-transferase 1A1 gene (UGT1A1) on c...
Subtle Mutation detection of SMN1 gene in Chinese SMA Patients:implication of Molecular Diagnostic P
[会议论文] 作者：JinLi Bai,YuJin Qu,YanYan Cao,Yan Li,WenHui Zhang,YuWei Jin,Hong Wang,Fang Song,EeZhen Li,LiWen Wang,,
来源：2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份：2014
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Subtle Mutation detection of SMN1 gene in Chinese SMA Patients:implication of Molecular Diagnostic P
[会议论文] 作者：JinLi Bai,YuJin Qu,YanYan Cao,EeZhen Li,LiWen Wang,Yan Li,YanLi Zhu,WenHui Zhang,YuWei Jin,Hong Wang,,
来源：2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份：2014
Background: Spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular disorder, which is caused by mutations of survival motor neuron 1 (SMN1) gene.Approximately 90-95％ of SMA patien...
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