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Ruen Yao

Showing results (61-70 of 66) with videos related to

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British Journal of Haematology|May 5, 2023
Germline Neurofibromin 1 mutation enhances the anti-tumour immune response and decreases juvenile myelomonocytic leukaemia tumourigenicityWanqiao Wang, Xin Li, Xia Qin, et al.
Eclinicalmedicine|June 24, 2022
Clinical characteristics and survival of children with hypertrophic cardiomyopathy in China: A multicentre retrospective cohort studyWenxiu Chan, Shiwei Yang, Jian Wang, et al.
European Journal of Human Genetics : EJHG|July 7, 2016
Estrogen-related receptor gamma implicated in a phenotype including hearing loss and mild developmental delaySamantha Lp Schilit, Benjamin B Currall, Ruen Yao, et al.
Ebiomedicine|December 28, 2023
Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital abnormalitiesNiu Li, Yufei Xu, Hongzhu Chen, et al.
Brain : a Journal of Neurology|March 4, 2023
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopmentFang Liu, Chen Liang, Zhengchang Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 6, 2021
CNV profiles of Chinese pediatric patients with developmental disordersHaiming Yuan, Shaofang Shangguan, Zhengchang Li, et al.
Pageof 7

Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 66 results.
British Journal of Haematology|May 5, 2023
Germline Neurofibromin 1 mutation enhances the anti-tumour immune response and decreases juvenile myelomonocytic leukaemia tumourigenicityWanqiao Wang, Xin Li, Xia Qin, et al.
Eclinicalmedicine|June 24, 2022
Clinical characteristics and survival of children with hypertrophic cardiomyopathy in China: A multicentre retrospective cohort studyWenxiu Chan, Shiwei Yang, Jian Wang, et al.
European Journal of Human Genetics : EJHG|July 7, 2016
Estrogen-related receptor gamma implicated in a phenotype including hearing loss and mild developmental delaySamantha Lp Schilit, Benjamin B Currall, Ruen Yao, et al.
Ebiomedicine|December 28, 2023
Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital abnormalitiesNiu Li, Yufei Xu, Hongzhu Chen, et al.
Brain : a Journal of Neurology|March 4, 2023
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopmentFang Liu, Chen Liang, Zhengchang Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 6, 2021
CNV profiles of Chinese pediatric patients with developmental disordersHaiming Yuan, Shaofang Shangguan, Zhengchang Li, et al.
Pageof 7