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Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
August 1, 2023
[A case of intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures caused by PHF21A gene variation and review of literature]
F Wu, X N Ji, M X Shen, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
June 12, 2020
[Clinical and genetic characteristics of children with STXBP1 encephalopathy]
J J Cao, X N Ji, Y Y Mao, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
June 29, 2023
[A case of combined oxidative phosphorylation deficiency 32 caused by MRPS34 gene variation and literature review]
M X Shen, X N Ji, F Wu, et al.
Zhonghua Yi Xue Za Zhi
|
November 16, 2018
[Study of <i>de novo</i> point mutations in known genes among patients with unexplained intellectual disability or developmental delay]
Z J Gao, Q Jiang, X L Chen, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
November 29, 2023
[Clinical characteristics of epileptic seizure in neurofibromatosis type 1 in 15 cases]
F Wu, X N Ji, M X Shen, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
November 1, 2019
[A phenotypic and genetic study on β-propeller protein-associated neurodegeneration]
W H Li, Q Chen, H Wang, et al.
Page
of 1
Search research articles
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Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
August 1, 2023
[A case of intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures caused by PHF21A gene variation and review of literature]
F Wu, X N Ji, M X Shen, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
June 12, 2020
[Clinical and genetic characteristics of children with STXBP1 encephalopathy]
J J Cao, X N Ji, Y Y Mao, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
June 29, 2023
[A case of combined oxidative phosphorylation deficiency 32 caused by MRPS34 gene variation and literature review]
M X Shen, X N Ji, F Wu, et al.
Zhonghua Yi Xue Za Zhi
|
November 16, 2018
[Study of <i>de novo</i> point mutations in known genes among patients with unexplained intellectual disability or developmental delay]
Z J Gao, Q Jiang, X L Chen, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
November 29, 2023
[Clinical characteristics of epileptic seizure in neurofibromatosis type 1 in 15 cases]
F Wu, X N Ji, M X Shen, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
November 1, 2019
[A phenotypic and genetic study on β-propeller protein-associated neurodegeneration]
W H Li, Q Chen, H Wang, et al.
Page
of 1