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Chuanchun Yang

Showing results (11-20 of 19) with videos related to

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Reproductive Biology and Endocrinology : RB&E|March 2, 2020
Successful pregnancy after prenatal diagnosis by NGS for a carrier of complex chromosome rearrangementsJian Ou, Chuanchun Yang, Xiaoli Cui, et al.
BMC Medical Genetics|July 25, 2016
Breakpoints and deleted genes identification of ring chromosome 18 in a Chinese girl by whole-genome low-coverage sequencing: a case report studyHui Yao, Chuanchun Yang, Xiaoli Huang, et al.
BMC Research Notes|February 17, 2026
Comparative analysis of four sequencing platforms for methylation sequencingJinxia Guan, Chuanchun Yang, Hongjun Gao, et al.
BMC Pediatrics|June 1, 2021
A de novo 10q11.23q22.1 deletion detected by whole genome mate-pair sequencing: a case reportDalin Fu, Weisheng Lin, Fen Lu, et al.
Medicine|February 17, 2021
A case report of congenital idiopathic hypogonadotropic hypogonadism caused by novel mutation of GNRHR geneLiping Wang, Weisheng Lin, Xiaohong Li, et al.
Genomics|August 3, 2014
Intragenic and extragenic disruptions of FOXL2 mapped by whole genome low-coverage sequencing in two BPES families with chromosome reciprocal translocationYongjia Yang, Chuanchun Yang, Yimin Zhu, et al.
Journal of Assisted Reproduction and Genetics|November 14, 2019
Screening of triploid with low-coverage whole-genome sequencing by a single-nucleotide polymorphism-based test in miscarriage tissueQian Geng, Xiaoli Cui, Yaqi Zhang, et al.
Annals of Translational Medicine|November 17, 2022
Systematic analysis of microbiota in pregnant Chinese women and its association with miscarriageYu Guang, Xiao Shen, Yan Tan, et al.
Human Mutation|March 11, 2014
A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencingZirui Dong, Lupin Jiang, Chuanchun Yang, et al.
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Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Reproductive Biology and Endocrinology : RB&E|March 2, 2020
Successful pregnancy after prenatal diagnosis by NGS for a carrier of complex chromosome rearrangementsJian Ou, Chuanchun Yang, Xiaoli Cui, et al.
BMC Medical Genetics|July 25, 2016
Breakpoints and deleted genes identification of ring chromosome 18 in a Chinese girl by whole-genome low-coverage sequencing: a case report studyHui Yao, Chuanchun Yang, Xiaoli Huang, et al.
BMC Research Notes|February 17, 2026
Comparative analysis of four sequencing platforms for methylation sequencingJinxia Guan, Chuanchun Yang, Hongjun Gao, et al.
BMC Pediatrics|June 1, 2021
A de novo 10q11.23q22.1 deletion detected by whole genome mate-pair sequencing: a case reportDalin Fu, Weisheng Lin, Fen Lu, et al.
Medicine|February 17, 2021
A case report of congenital idiopathic hypogonadotropic hypogonadism caused by novel mutation of GNRHR geneLiping Wang, Weisheng Lin, Xiaohong Li, et al.
Genomics|August 3, 2014
Intragenic and extragenic disruptions of FOXL2 mapped by whole genome low-coverage sequencing in two BPES families with chromosome reciprocal translocationYongjia Yang, Chuanchun Yang, Yimin Zhu, et al.
Journal of Assisted Reproduction and Genetics|November 14, 2019
Screening of triploid with low-coverage whole-genome sequencing by a single-nucleotide polymorphism-based test in miscarriage tissueQian Geng, Xiaoli Cui, Yaqi Zhang, et al.
Annals of Translational Medicine|November 17, 2022
Systematic analysis of microbiota in pregnant Chinese women and its association with miscarriageYu Guang, Xiao Shen, Yan Tan, et al.
Human Mutation|March 11, 2014
A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencingZirui Dong, Lupin Jiang, Chuanchun Yang, et al.
Pageof 2