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Qiaoli Li

Showing results (171-180 of 208) with videos related to

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Human Molecular Genetics|July 4, 2014
Ildr1b is essential for semicircular canal development, migration of the posterior lateral line primordium and hearing ability in zebrafish: implications for a role in the recessive hearing impairment DFNB42Qing Sang, Junyu Zhang, Ruizhi Feng, et al.
American Journal of Human Genetics|April 3, 2018
Homozygous Mutations in WEE2 Cause Fertilization Failure and Female InfertilityQing Sang, Bin Li, Yanping Kuang, et al.
Human Genetics|March 30, 2023
ADGB variants cause asthenozoospermia and male infertilityRonggui Qu, Zhihua Zhang, Ling Wu, et al.
American Journal of Human Genetics|October 1, 2013
Cole Disease Results from Mutations in ENPP1Ori Eytan, Fanny Morice-Picard, Ofer Sarig, et al.
Rheumatology (Oxford, England)|June 21, 2021
Inorganic pyrophosphate is reduced in patients with systemic sclerosisVivien M Hsu, Eszter Kozák, Qiaoli Li, et al.
Frontiers in Endocrinology|June 8, 2026
Therapeutic efficacy of glucocorticoids, ATP, and antithyroid drugs in acute thyrotoxic myopathy: evaluation using the acute thyrotoxic myopathy symptom scoreQiaoli Li, Xuelan Chen, Zien Huang, et al.
Human Genetics|January 22, 2024
Bi-allelic missense variants in MEI4 cause preimplantation embryonic arrest and female infertilityZhiqi Pan, Weijie Wang, Ling Wu, et al.
Human Reproduction (Oxford, England)|May 30, 2021
FBXO43 variants in patients with female infertility characterized by early embryonic arrestWeijie Wang, Wenjing Wang, Yao Xu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Genetic heterogeneity of heritable ectopic mineralization disorders in a large international cohortAmir Hossein Saeidian, Leila Youssefian, Jianhe Huang, et al.
American Journal of Human Genetics|October 3, 2017
Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation ArrestBiaobang Chen, Zhihua Zhang, Xiaoxi Sun, et al.
Pageof 21

Showing results (171-180 of 208) with videos related to

Sort By:
Pageof 21
Human Molecular Genetics|July 4, 2014
Ildr1b is essential for semicircular canal development, migration of the posterior lateral line primordium and hearing ability in zebrafish: implications for a role in the recessive hearing impairment DFNB42Qing Sang, Junyu Zhang, Ruizhi Feng, et al.
American Journal of Human Genetics|April 3, 2018
Homozygous Mutations in WEE2 Cause Fertilization Failure and Female InfertilityQing Sang, Bin Li, Yanping Kuang, et al.
Human Genetics|March 30, 2023
ADGB variants cause asthenozoospermia and male infertilityRonggui Qu, Zhihua Zhang, Ling Wu, et al.
American Journal of Human Genetics|October 1, 2013
Cole Disease Results from Mutations in ENPP1Ori Eytan, Fanny Morice-Picard, Ofer Sarig, et al.
Rheumatology (Oxford, England)|June 21, 2021
Inorganic pyrophosphate is reduced in patients with systemic sclerosisVivien M Hsu, Eszter Kozák, Qiaoli Li, et al.
Frontiers in Endocrinology|June 8, 2026
Therapeutic efficacy of glucocorticoids, ATP, and antithyroid drugs in acute thyrotoxic myopathy: evaluation using the acute thyrotoxic myopathy symptom scoreQiaoli Li, Xuelan Chen, Zien Huang, et al.
Human Genetics|January 22, 2024
Bi-allelic missense variants in MEI4 cause preimplantation embryonic arrest and female infertilityZhiqi Pan, Weijie Wang, Ling Wu, et al.
Human Reproduction (Oxford, England)|May 30, 2021
FBXO43 variants in patients with female infertility characterized by early embryonic arrestWeijie Wang, Wenjing Wang, Yao Xu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Genetic heterogeneity of heritable ectopic mineralization disorders in a large international cohortAmir Hossein Saeidian, Leila Youssefian, Jianhe Huang, et al.
American Journal of Human Genetics|October 3, 2017
Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation ArrestBiaobang Chen, Zhihua Zhang, Xiaoxi Sun, et al.
Pageof 21