Baoheng Gui Shenzhen Research Institute The Chinese University of Hong Kong Biography Publications Institution JoVE Articles Baoheng Gui has not added a biography. If you are Baoheng Gui and would like to personalize this page please email our Author Liaison for assistance. Publications Low-pass Genome Sequencing Versus Chromosomal Microarray Analysis: Implementation in Prenatal Diagnosis Genetics in Medicine : Official Journal of the American College of Medical Genetics. Aug, 2019 | Pubmed ID: 31447483 A Prospective Study of Non-invasive Preimplantation Genetic Testing for Aneuploidies (NiPGT-A) Using Next-generation Sequencing (NGS) on Spent Culture Media (SCM) Journal of Assisted Reproduction and Genetics. Jul, 2019 | Pubmed ID: 31292818 New Insights into 5α-reductase Type 2 Deficiency Based on a Multi-centre Study: Regional Distribution and Genotype-phenotype Profiling of in 190 Chinese Patients Journal of Medical Genetics. Jun, 2019 | Pubmed ID: 31186340 Reply to Lutz-Bonengel Et Al.: Biparental MtDNA Transmission is Unlikely to Be the Result of Nuclear Mitochondrial DNA Segments Proceedings of the National Academy of Sciences of the United States of America. 02, 2019 | Pubmed ID: 30674682 Biparental Inheritance of Mitochondrial DNA in Humans Proceedings of the National Academy of Sciences of the United States of America. 12, 2018 | Pubmed ID: 30478036 Novel Pathogenic RECQL4 Variants in Chinese Patients with Rothmund-Thomson Syndrome Gene. May, 2018 | Pubmed ID: 29462647 Perspective: Is Random Monoallelic Expression a Contributor to Phenotypic Variability of Autosomal Dominant Disorders? Frontiers in Genetics. 2017 | Pubmed ID: 29250101 Biallelic Mutations in the Ferredoxin Reductase Gene Cause Novel Mitochondriopathy with Optic Atrophy Human Molecular Genetics. 12, 2017 | Pubmed ID: 29040572 Prenatal and Early Diagnosis of Chinese 3-M Syndrome Patients with Novel Pathogenic Variants Clinica Chimica Acta; International Journal of Clinical Chemistry. Nov, 2017 | Pubmed ID: 28969986 Next-generation Sequencing Analysis of TSHR in 384 Chinese Subclinical Congenital Hypothyroidism (CH) and CH Patients Clinica Chimica Acta; International Journal of Clinical Chemistry. Nov, 2016 | Pubmed ID: 27637299 Робуст Полимераза Цепная реакция на основе Ассаем для количественной цитозин-гуанин-гуанин тринуклеотид повторяет в хрупкой X умственной отсталости-1 Гена Huilin Wang*1, Xiaofan Zhu*2,3, Baoheng Gui*3,4, Wan Chee Cheung2, Mengmeng Shi2,3, Zhenjun Yang2,3, Ka Yin Kwok2, Ricky Lim5, Sanna Pietilä5, Yuanfang Zhu6,7, Kwong Wai Choy2,3 1Central Laboratory, Bao'an Maternity and Child Health Hospital, Jinan University, 2Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, 3Shenzhen Research Institute, The Chinese University of Hong Kong, 4Department of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, 5PerkinElmer Diagnostics, 6Department of Obstetrics and Gynecology, Bao'an Maternity and Child Health Hospital, Jinan University, 7Maternal-Fetal Medicine Institute, Bao'an Maternity and Child Health Hospital, Jinan University JoVE 59963 Genetics Полупроводниковое секвенирование для предимплантационного генетического тестирования на анеуплоидию Baoheng Gui*1,2,3, Yingxin Zhang*4, Bo Liang5, Yvonne Ka Yin Kwok4, Wai Ting Lui4, Queenie Sum Yee Yeung4, Lingyin Kong6, Liming Xuan6, Jacqueline Pui Wah Chung4, Kwong Wai Choy3,4 1Department of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, 2Birth Defects Prevention and Control Institute of Guangxi Zhuang Autonomous Region, 3Shenzhen Research Institute, The Chinese University of Hong Kong, 4Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, 5State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic and Developmental Sciences, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, 6Basecare Medical Device Co., Ltd JoVE 59273 Genetics
Робуст Полимераза Цепная реакция на основе Ассаем для количественной цитозин-гуанин-гуанин тринуклеотид повторяет в хрупкой X умственной отсталости-1 Гена Huilin Wang*1, Xiaofan Zhu*2,3, Baoheng Gui*3,4, Wan Chee Cheung2, Mengmeng Shi2,3, Zhenjun Yang2,3, Ka Yin Kwok2, Ricky Lim5, Sanna Pietilä5, Yuanfang Zhu6,7, Kwong Wai Choy2,3 1Central Laboratory, Bao'an Maternity and Child Health Hospital, Jinan University, 2Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, 3Shenzhen Research Institute, The Chinese University of Hong Kong, 4Department of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, 5PerkinElmer Diagnostics, 6Department of Obstetrics and Gynecology, Bao'an Maternity and Child Health Hospital, Jinan University, 7Maternal-Fetal Medicine Institute, Bao'an Maternity and Child Health Hospital, Jinan University JoVE 59963 Genetics
Полупроводниковое секвенирование для предимплантационного генетического тестирования на анеуплоидию Baoheng Gui*1,2,3, Yingxin Zhang*4, Bo Liang5, Yvonne Ka Yin Kwok4, Wai Ting Lui4, Queenie Sum Yee Yeung4, Lingyin Kong6, Liming Xuan6, Jacqueline Pui Wah Chung4, Kwong Wai Choy3,4 1Department of Genetics and Metabolism, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, 2Birth Defects Prevention and Control Institute of Guangxi Zhuang Autonomous Region, 3Shenzhen Research Institute, The Chinese University of Hong Kong, 4Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, 5State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic and Developmental Sciences, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, 6Basecare Medical Device Co., Ltd JoVE 59273 Genetics
