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Fertility and Sterility
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February 19, 2021
Clinical characteristics and molecular genetics of complete androgen insensitivity syndrome patients: a series study of 30 cases from a Chinese tertiary medical center
Duoduo Zhang, Fengxia Yao, Tiffany Tian, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
September 8, 2012
CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiency
Fengxia Yao, Shangzhi Huang, Xiaodi Kang, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
June 6, 2009
Genotyping of a Chinese family with 46,XX and 46,XY 17-hydroxylase deficiency
Qinjie Tian, Fengxia Yao, Guihua Sha, et al.
BMC Nephrology
|
December 13, 2021
A novel MAGED2 variant in a Chinese preterm newborn with transient antenatal Bartter's syndrome with 4 years follow-up
Mingsheng Ma, Mengqi Zhang, Yu Zhou, et al.
Gene
|
June 20, 2017
Clinical and genetic characteristics of 17 Chinese patients with glycogen storage disease type IXa
Jiangwei Zhang, Yuheng Yuan, Mingsheng Ma, et al.
Frontiers in Endocrinology
|
January 2, 2023
Clinical characteristics and molecular etiology of partial 17α-hydroxylase deficiency diagnosed in 46,XX patients
Duoduo Zhang, Fengxia Yao, Min Luo, et al.
Ophthalmic Genetics
|
September 5, 2013
De novo mutations in the cone-rod homeobox gene associated with leber congenital amaurosis in Chinese patients
Xuan Zou, Fengxia Yao, Xiaofang Liang, et al.
International Journal of General Medicine
|
August 26, 2022
Genotype-Phenotype Correlation Analysis and Identification of a Novel <i>SRD5A2</i> Mutation in Four Unrelated Chinese Patients with 5α-Reductase Deficiency
Ting Gui, Fengxia Yao, Xinzhuang Yang, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
January 13, 2026
Alpha-mannosidosis due to a novel MAN2B1 truncating mutation in a Chinese patient: a new report and long-term follow-up
Fengxia Yao, Yamei Li, Xing Wei, et al.
Nucleic Acids Research
|
June 28, 2005
SNP Cutter: a comprehensive tool for SNP PCR-RFLP assay design
Ruifang Zhang, Zanhua Zhu, Hongming Zhu, et al.
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of 4
Search research articles
Search
Showing results (11-20 of 34) with videos related to
Sort By:
Page
of 4
Fertility and Sterility
|
February 19, 2021
Clinical characteristics and molecular genetics of complete androgen insensitivity syndrome patients: a series study of 30 cases from a Chinese tertiary medical center
Duoduo Zhang, Fengxia Yao, Tiffany Tian, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
September 8, 2012
CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiency
Fengxia Yao, Shangzhi Huang, Xiaodi Kang, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
June 6, 2009
Genotyping of a Chinese family with 46,XX and 46,XY 17-hydroxylase deficiency
Qinjie Tian, Fengxia Yao, Guihua Sha, et al.
BMC Nephrology
|
December 13, 2021
A novel MAGED2 variant in a Chinese preterm newborn with transient antenatal Bartter's syndrome with 4 years follow-up
Mingsheng Ma, Mengqi Zhang, Yu Zhou, et al.
Gene
|
June 20, 2017
Clinical and genetic characteristics of 17 Chinese patients with glycogen storage disease type IXa
Jiangwei Zhang, Yuheng Yuan, Mingsheng Ma, et al.
Frontiers in Endocrinology
|
January 2, 2023
Clinical characteristics and molecular etiology of partial 17α-hydroxylase deficiency diagnosed in 46,XX patients
Duoduo Zhang, Fengxia Yao, Min Luo, et al.
Ophthalmic Genetics
|
September 5, 2013
De novo mutations in the cone-rod homeobox gene associated with leber congenital amaurosis in Chinese patients
Xuan Zou, Fengxia Yao, Xiaofang Liang, et al.
International Journal of General Medicine
|
August 26, 2022
Genotype-Phenotype Correlation Analysis and Identification of a Novel <i>SRD5A2</i> Mutation in Four Unrelated Chinese Patients with 5α-Reductase Deficiency
Ting Gui, Fengxia Yao, Xinzhuang Yang, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
January 13, 2026
Alpha-mannosidosis due to a novel MAN2B1 truncating mutation in a Chinese patient: a new report and long-term follow-up
Fengxia Yao, Yamei Li, Xing Wei, et al.
Nucleic Acids Research
|
June 28, 2005
SNP Cutter: a comprehensive tool for SNP PCR-RFLP assay design
Ruifang Zhang, Zanhua Zhu, Hongming Zhu, et al.
Page
of 4