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Haibo Mei

Showing results (131-140 of 138) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2022
MECOM-related disorder: Radioulnar synostosis without hematological aberration due to unique variantsFang Shen, Yongjia Yang, Yu Zheng, et al.
Journal of Children'S Orthopaedics|July 30, 2025
All-inside physeal bar resection for partial physeal arrest of the distal radius with the aid of an arthroscope and patient-specific instrumentHan Xiao, Baohui Xiao, Xiaoqian Tan, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 3, 2020
Tailor-Made Amino Acids and Fluorinated Motifs as Prominent Traits in Modern PharmaceuticalsHaibo Mei, Jianlin Han, Sarah White, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 31, 2011
A novel mutation leading to elongation of the deduced α1(X) chain results in Metaphyseal Chondrodysplasia type SchmidYimin Zhu, Liping Li, Lijun Zhou, et al.
Chemical Reviews|March 16, 2021
Chemical Aspects of Human and Environmental Overload with FluorineJianlin Han, Loránd Kiss, Haibo Mei, et al.
Orphanet Journal of Rare Diseases|September 20, 2019
Identification and characterization of NF1 and non-NF1 congenital pseudarthrosis of the tibia based on germline NF1 variants: genetic and clinical analysis of 75 patientsGuanghui Zhu, Yu Zheng, Yaoxi Liu, et al.
Oncotarget|April 19, 2017
BMPR1B mutation causes Pierre Robin sequenceYongjia Yang, Jianying Yuan, Xu Yao, et al.
Human Molecular Genetics|July 28, 2025
Long-read sequencing for NF1 gene analysis: enhancing diagnostic accuracy for Neurofibromatosis type 1Yu Zheng, Miaomiao Chen, Shuju Zhang, et al.
Pageof 14

Showing results (131-140 of 138) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 138 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2022
MECOM-related disorder: Radioulnar synostosis without hematological aberration due to unique variantsFang Shen, Yongjia Yang, Yu Zheng, et al.
Journal of Children'S Orthopaedics|July 30, 2025
All-inside physeal bar resection for partial physeal arrest of the distal radius with the aid of an arthroscope and patient-specific instrumentHan Xiao, Baohui Xiao, Xiaoqian Tan, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 3, 2020
Tailor-Made Amino Acids and Fluorinated Motifs as Prominent Traits in Modern PharmaceuticalsHaibo Mei, Jianlin Han, Sarah White, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 31, 2011
A novel mutation leading to elongation of the deduced α1(X) chain results in Metaphyseal Chondrodysplasia type SchmidYimin Zhu, Liping Li, Lijun Zhou, et al.
Chemical Reviews|March 16, 2021
Chemical Aspects of Human and Environmental Overload with FluorineJianlin Han, Loránd Kiss, Haibo Mei, et al.
Orphanet Journal of Rare Diseases|September 20, 2019
Identification and characterization of NF1 and non-NF1 congenital pseudarthrosis of the tibia based on germline NF1 variants: genetic and clinical analysis of 75 patientsGuanghui Zhu, Yu Zheng, Yaoxi Liu, et al.
Oncotarget|April 19, 2017
BMPR1B mutation causes Pierre Robin sequenceYongjia Yang, Jianying Yuan, Xu Yao, et al.
Human Molecular Genetics|July 28, 2025
Long-read sequencing for NF1 gene analysis: enhancing diagnostic accuracy for Neurofibromatosis type 1Yu Zheng, Miaomiao Chen, Shuju Zhang, et al.
Pageof 14