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Shaoke Chen

Showing results (41-50 of 80) with videos related to

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Scientific Reports|January 18, 2018
Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonatesChunyun Fu, Shiyu Luo, Qifei Li, et al.
Journal of Paediatrics and Child Health|August 9, 2020
High prevalence of elevated serum liver enzymes in Chinese children suggests metabolic syndrome as a common risk factorJinling Wang, Hui-Qi Qu, Ke Huang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 25, 2016
Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patientsChunyun Fu, Shiyu Luo, Shujie Zhang, et al.
Gene|February 21, 2018
Novel pathogenic RECQL4 variants in Chinese patients with Rothmund-Thomson syndromeBaoheng Gui, Yanning Song, Xuyun Hu, et al.
Human Genomics|September 16, 2024
The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mappingYunting Ma, Chunrong Gui, Meizhen Shi, et al.
Biology of Sex Differences|February 12, 2026
A hypomorphic SRD5A2 haplotype with a potential founder effect: composed of common variants in individuals with 5α-reductase type 2 deficiency from South ChinaXiaoyun Lei, Xu Zhou, Zifeng Cheng, et al.
Childhood Obesity (Print)|August 14, 2019
Parental Perceptions of Obesity in School Children and Subsequent ActionÉadaoin M Butler, Alisha Suhag, Ye Hong, et al.
Orphanet Journal of Rare Diseases|March 29, 2022
Delineation of dual molecular diagnosis in patients with skeletal deformityLian Liu, Liying Sun, Yujun Chen, et al.
Plos One|August 12, 2014
The effects of genetic variation in FTO rs9939609 on obesity and dietary preferences in Chinese Han children and adolescentsMin Yang, Yuyang Xu, Li Liang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 4, 2017
Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variantsXuyun Hu, Hongdou Li, Baoheng Gui, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Scientific Reports|January 18, 2018
Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonatesChunyun Fu, Shiyu Luo, Qifei Li, et al.
Journal of Paediatrics and Child Health|August 9, 2020
High prevalence of elevated serum liver enzymes in Chinese children suggests metabolic syndrome as a common risk factorJinling Wang, Hui-Qi Qu, Ke Huang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 25, 2016
Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patientsChunyun Fu, Shiyu Luo, Shujie Zhang, et al.
Gene|February 21, 2018
Novel pathogenic RECQL4 variants in Chinese patients with Rothmund-Thomson syndromeBaoheng Gui, Yanning Song, Xuyun Hu, et al.
Human Genomics|September 16, 2024
The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mappingYunting Ma, Chunrong Gui, Meizhen Shi, et al.
Biology of Sex Differences|February 12, 2026
A hypomorphic SRD5A2 haplotype with a potential founder effect: composed of common variants in individuals with 5α-reductase type 2 deficiency from South ChinaXiaoyun Lei, Xu Zhou, Zifeng Cheng, et al.
Childhood Obesity (Print)|August 14, 2019
Parental Perceptions of Obesity in School Children and Subsequent ActionÉadaoin M Butler, Alisha Suhag, Ye Hong, et al.
Orphanet Journal of Rare Diseases|March 29, 2022
Delineation of dual molecular diagnosis in patients with skeletal deformityLian Liu, Liying Sun, Yujun Chen, et al.
Plos One|August 12, 2014
The effects of genetic variation in FTO rs9939609 on obesity and dietary preferences in Chinese Han children and adolescentsMin Yang, Yuyang Xu, Li Liang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 4, 2017
Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variantsXuyun Hu, Hongdou Li, Baoheng Gui, et al.
Pageof 8