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Frontiers in Pediatrics
|
January 21, 2026
Expansion of the genetic and phenotypic spectrum of hereditary spastic paraplegia caused by <i>ABHD16A</i> gene variants: an integrated analysis based on novel variants and literature review
Manling He, Qiang Zhang, Shaoke Chen, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
September 12, 2013
[Epidemiologic study on current pubertal development in Chinese school-aged children]
Mingqiang Zhu, Junfen Fu, Li Liang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 10, 2016
[Identification of two novel mutations of MUT gene in a Chinese family affected with isolated methylmalonic acidemia]
Bobo Xie, Jingsi Luo, Xin Fan, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi
|
November 8, 2014
[A proposal for the cutoff point of waist-to-height for the diagnosis of metabolic syndrome in children and adolescents in six areas of China]
Yangli Dai, Junfen Fu, Li Liang, et al.
Global Pediatric Health
|
June 24, 2016
Incidence and Interrelated Factors in Patients With Congenital Hypothyroidism as Detected by Newborn Screening in Guangxi, China
Xin Fan, Shaoke Chen, Jiale Qian, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi
|
August 26, 2014
[Genotypes of 1 571 cases of Hb H disease in Guangxi area]
Chunyun Fu, Shaoke Chen, Qiang Zhang, et al.
Scientific Reports
|
July 2, 2025
Genetic skeletal disorders: phenotypic-genotypic characteristics and RhGH therapy responses of a pediatric cohort
Yiyun Huang, Yan Peng, Chuan Li, et al.
BMC Medical Genetics
|
May 1, 2015
EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndrome
Chuan Li, Rongyu Chen, Xin Fan, et al.
Journal of Human Genetics
|
March 15, 2013
Genetic effects have a dominant role on poor responses to infant vaccination to hepatitis B virus
Kai Yan, Wenping Cai, Fang Cao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
September 1, 2016
[A novel compound heterozygous mutation causing 3-methylcrotonyl-CoA carboxylase deficiency]
Bobo Xie, Jingsi Luo, Yaqin Lei, et al.
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Search research articles
Search
Showing results (11-20 of 80) with videos related to
Sort By:
Page
of 8
Frontiers in Pediatrics
|
January 21, 2026
Expansion of the genetic and phenotypic spectrum of hereditary spastic paraplegia caused by <i>ABHD16A</i> gene variants: an integrated analysis based on novel variants and literature review
Manling He, Qiang Zhang, Shaoke Chen, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
September 12, 2013
[Epidemiologic study on current pubertal development in Chinese school-aged children]
Mingqiang Zhu, Junfen Fu, Li Liang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 10, 2016
[Identification of two novel mutations of MUT gene in a Chinese family affected with isolated methylmalonic acidemia]
Bobo Xie, Jingsi Luo, Xin Fan, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi
|
November 8, 2014
[A proposal for the cutoff point of waist-to-height for the diagnosis of metabolic syndrome in children and adolescents in six areas of China]
Yangli Dai, Junfen Fu, Li Liang, et al.
Global Pediatric Health
|
June 24, 2016
Incidence and Interrelated Factors in Patients With Congenital Hypothyroidism as Detected by Newborn Screening in Guangxi, China
Xin Fan, Shaoke Chen, Jiale Qian, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi
|
August 26, 2014
[Genotypes of 1 571 cases of Hb H disease in Guangxi area]
Chunyun Fu, Shaoke Chen, Qiang Zhang, et al.
Scientific Reports
|
July 2, 2025
Genetic skeletal disorders: phenotypic-genotypic characteristics and RhGH therapy responses of a pediatric cohort
Yiyun Huang, Yan Peng, Chuan Li, et al.
BMC Medical Genetics
|
May 1, 2015
EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndrome
Chuan Li, Rongyu Chen, Xin Fan, et al.
Journal of Human Genetics
|
March 15, 2013
Genetic effects have a dominant role on poor responses to infant vaccination to hepatitis B virus
Kai Yan, Wenping Cai, Fang Cao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
September 1, 2016
[A novel compound heterozygous mutation causing 3-methylcrotonyl-CoA carboxylase deficiency]
Bobo Xie, Jingsi Luo, Yaqin Lei, et al.
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of 8