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Chuanchun Yang

Showing results (1-10 of 19) with videos related to

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Clinical Laboratory|May 9, 2018
Serum CEA and CA19-9 Levels are Associated with the Presence and Severity of Colorectal NeoplasiaHengyong Zhai, Junxing Huang, Chuanchun Yang, et al.
Clinical Laboratory|April 18, 2021
Breakpoints Identification of a Balanced Complex Chromosome Rearrangement Case: 46,XX, t(6;15;10;9)(q13;q15;p11.2;q34.3) ins(9;8)(q22.33;q21.1q21.3)Bohong Li, Suli Li, Fuwei Luo, et al.
Journal of Cellular and Molecular Medicine|July 29, 2022
Highly precise breakpoint detection of chromosome balanced translocation in chronic myelogenous leukaemia: Case seriesChuanchun Yang, Xiaoli Cui, Lei Xu, et al.
Molecular Cytogenetics|May 19, 2022
Analysis of complex chromosomal rearrangements using a combination of current molecular cytogenetic techniquesPing He, Xiaoni Wei, Yuchan Xu, et al.
Gene|June 18, 2014
Mapping breakpoints of a familial chromosome insertion (18,7) (q22.1; q36.2q21.11) to DPP6 and CACNA2D1 genes in an azoospermic maleLin Li, Haixiao Chen, Chenxing Yin, et al.
Journal of Medical Genetics|July 16, 2025
<i>AUTS2</i> disruption underlies radioulnar synostosis and skeletal dysmorphogenesis: evidence from four unrelated casesCheng Liu, Fang Shen, Mei Deng, et al.
Reproductive Biology and Endocrinology : RB&E|April 21, 2021
Successful birth after preimplantation genetic testing for a couple with two different reciprocal translocations and review of the literatureDun Liu, Chuangqi Chen, Xiqian Zhang, et al.
Plos One|May 25, 2016
Mapping Breakpoints of Complex Chromosome Rearrangements Involving a Partial Trisomy 15q23.1-q26.2 Revealed by Next Generation Sequencing and Conventional TechniquesQiong Pan, Hao Hu, Liangrong Han, et al.
Molecular Cytogenetics|April 12, 2018
Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblingsAixiang Luo, Dehua Cheng, Shimin Yuan, et al.
Journal of Human Genetics|July 12, 2013
Complete genome sequencing and variant analysis of a Pakistani individualMuhammad Kamran Azim, Chuanchun Yang, Zhixiang Yan, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Clinical Laboratory|May 9, 2018
Serum CEA and CA19-9 Levels are Associated with the Presence and Severity of Colorectal NeoplasiaHengyong Zhai, Junxing Huang, Chuanchun Yang, et al.
Clinical Laboratory|April 18, 2021
Breakpoints Identification of a Balanced Complex Chromosome Rearrangement Case: 46,XX, t(6;15;10;9)(q13;q15;p11.2;q34.3) ins(9;8)(q22.33;q21.1q21.3)Bohong Li, Suli Li, Fuwei Luo, et al.
Journal of Cellular and Molecular Medicine|July 29, 2022
Highly precise breakpoint detection of chromosome balanced translocation in chronic myelogenous leukaemia: Case seriesChuanchun Yang, Xiaoli Cui, Lei Xu, et al.
Molecular Cytogenetics|May 19, 2022
Analysis of complex chromosomal rearrangements using a combination of current molecular cytogenetic techniquesPing He, Xiaoni Wei, Yuchan Xu, et al.
Gene|June 18, 2014
Mapping breakpoints of a familial chromosome insertion (18,7) (q22.1; q36.2q21.11) to DPP6 and CACNA2D1 genes in an azoospermic maleLin Li, Haixiao Chen, Chenxing Yin, et al.
Journal of Medical Genetics|July 16, 2025
<i>AUTS2</i> disruption underlies radioulnar synostosis and skeletal dysmorphogenesis: evidence from four unrelated casesCheng Liu, Fang Shen, Mei Deng, et al.
Reproductive Biology and Endocrinology : RB&E|April 21, 2021
Successful birth after preimplantation genetic testing for a couple with two different reciprocal translocations and review of the literatureDun Liu, Chuangqi Chen, Xiqian Zhang, et al.
Plos One|May 25, 2016
Mapping Breakpoints of Complex Chromosome Rearrangements Involving a Partial Trisomy 15q23.1-q26.2 Revealed by Next Generation Sequencing and Conventional TechniquesQiong Pan, Hao Hu, Liangrong Han, et al.
Molecular Cytogenetics|April 12, 2018
Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblingsAixiang Luo, Dehua Cheng, Shimin Yuan, et al.
Journal of Human Genetics|July 12, 2013
Complete genome sequencing and variant analysis of a Pakistani individualMuhammad Kamran Azim, Chuanchun Yang, Zhixiang Yan, et al.
Pageof 2