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Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
October 15, 2013
[Analysis of GALNS gene mutation in thirty-eight Chinese patients with mucopolysaccharidosis type IVA]
Jun Ye, Hong-lin Lei, Hui-wen Zhang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
December 3, 2009
[Molecular genetic analysis of 10 Chinese patients with glycogen storage disease type III]
Xia Wang, Wen-juan Qiu, Jun Ye, et al.
Acta Pharmacologica Sinica
|
June 7, 2018
Identification of predominant GNPTAB gene mutations in Eastern Chinese patients with mucolipidosis II/III and a prenatal diagnosis of mucolipidosis II
Yu Wang, Jun Ye, Wen-Juan Qiu, et al.
World Journal of Pediatrics : WJP
|
May 8, 2014
Clinical features and mutations in seven Chinese patients with very long chain acyl-CoA dehydrogenase deficiency
Rui-Nan Zhang, Yi-Fan Li, Wen-Juan Qiu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
June 7, 2011
[Application of enzyme assay and gene analysis in the prenatal diagnosis for a family with glycogen storage disease type II]
Min-hui Zeng, Wen-juan Qiu, Xue-fan Gu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
April 30, 2010
[Clinical diagnosis and WISP3 gene mutation analysis for progressive pseudorheumatoid dysplasia]
Jun Ye, Hui-wen Zhang, Tong Wang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
December 23, 2008
[Diagnosis, treatment and gene mutation analysis of the first case with dihydropteridine reductase deficiency in the mainland of China]
Jun Ye, Wen-juan Qiu, Lian-shu Han, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
June 9, 2007
[Clinical study of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency in southern and northern Chinese patients]
Ling Yang, Zhi-xin Zhang, Jun Ye, et al.
Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]
|
August 22, 2007
[Diagnosis, treatment and long-term following up of 223 patients with hyperphenylalaninemia detected by neonatal screening programs]
Jun Ye, Wen-juan Qiu, Lian-shu Han, et al.
World Journal of Pediatrics : WJP
|
October 12, 2015
Clinical features and MUT gene mutation spectrum in Chinese patients with isolated methylmalonic acidemia: identification of ten novel allelic variants
Lian-Shu Han, Zhuo Huang, Feng Han, et al.
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of 8
Search research articles
Search
Showing results (41-50 of 71) with videos related to
Sort By:
Page
of 8
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
October 15, 2013
[Analysis of GALNS gene mutation in thirty-eight Chinese patients with mucopolysaccharidosis type IVA]
Jun Ye, Hong-lin Lei, Hui-wen Zhang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
December 3, 2009
[Molecular genetic analysis of 10 Chinese patients with glycogen storage disease type III]
Xia Wang, Wen-juan Qiu, Jun Ye, et al.
Acta Pharmacologica Sinica
|
June 7, 2018
Identification of predominant GNPTAB gene mutations in Eastern Chinese patients with mucolipidosis II/III and a prenatal diagnosis of mucolipidosis II
Yu Wang, Jun Ye, Wen-Juan Qiu, et al.
World Journal of Pediatrics : WJP
|
May 8, 2014
Clinical features and mutations in seven Chinese patients with very long chain acyl-CoA dehydrogenase deficiency
Rui-Nan Zhang, Yi-Fan Li, Wen-Juan Qiu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
June 7, 2011
[Application of enzyme assay and gene analysis in the prenatal diagnosis for a family with glycogen storage disease type II]
Min-hui Zeng, Wen-juan Qiu, Xue-fan Gu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
April 30, 2010
[Clinical diagnosis and WISP3 gene mutation analysis for progressive pseudorheumatoid dysplasia]
Jun Ye, Hui-wen Zhang, Tong Wang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
December 23, 2008
[Diagnosis, treatment and gene mutation analysis of the first case with dihydropteridine reductase deficiency in the mainland of China]
Jun Ye, Wen-juan Qiu, Lian-shu Han, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
June 9, 2007
[Clinical study of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency in southern and northern Chinese patients]
Ling Yang, Zhi-xin Zhang, Jun Ye, et al.
Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]
|
August 22, 2007
[Diagnosis, treatment and long-term following up of 223 patients with hyperphenylalaninemia detected by neonatal screening programs]
Jun Ye, Wen-juan Qiu, Lian-shu Han, et al.
World Journal of Pediatrics : WJP
|
October 12, 2015
Clinical features and MUT gene mutation spectrum in Chinese patients with isolated methylmalonic acidemia: identification of ten novel allelic variants
Lian-Shu Han, Zhuo Huang, Feng Han, et al.
Page
of 8