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Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|May 29, 2008
[Mutation analysis and one novel mutation detection of 6-pyruvoyl tetrahydropterin synthase gene in children with tetrahydrobiopterin deficiency]Yu-Jin Qu, Fang Song, Yu-Wei Jin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 13, 2006
[Detection of the prevalent mutations of 6-pyruvoyl-tetrahydropterin synthase gene by PCR-RFLP analysis in Chinese patients]Yu-jin Qu, Fang Song, Hong Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 8, 2012
[Limitation of PCR-RFLP method for the detection of genetic mutations in spinal muscular atrophy]Yu-wei Jin, Yu-jin Qu, Hong Wang, et al.
Chinese Medical Journal|March 3, 2011
Compound heterozygous mutation in two unrelated cases of Chinese spinal muscular atrophy patientsYu-Jin Qu, Fang Song, Yan-Ling Yang, et al.
Molecular Genetics and Metabolism|November 1, 2005
Phenylketonuria mutations in Northern ChinaFang Song, Yu-jin Qu, Ting Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 7, 2009
[A study on genetic diagnosis for Angelman syndrome]Li-jun Liu, Jin-li Bai, Yu-jin Qu, et al.
Chinese Medical Journal|March 3, 2011
A novel missense mutation of the ubiquitin protein ligase E3A gene in a patient with Angelman syndromeJin-Li Bai, Yu-Jin Qu, Li-Ping Zou, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|December 23, 2008
[Spectrum of phenylalanine hydroxylase gene mutations and genotype-phenotype correlation in the patients with phenylketonuria in Beijing area of China]Yu-jin Qu, Fang Song, Yu-wei Jin, et al.
Molecular Genetics and Metabolism|December 3, 2014
Fast clinical molecular diagnosis of hyperphenylalaninemia using next-generation sequencing-based on a custom AmpliSeq™ panel and Ion Torrent PGM sequencingYan-yan Cao, Yu-jin Qu, Fang Song, et al.
Zhonghua Yi Xue Za Zhi|October 11, 2008
[Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a reliable method for detection of non-homozygous patients with spinal muscular atrophy]Mei-juan Long, Fang Song, Yu-jin Qu, et al.
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