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Journal of Assisted Reproduction and Genetics
|
December 15, 2023
Identification of cryptic balanced translocations in couples with unexplained recurrent pregnancy loss based upon embryonic PGT-A results
Shuo Li, Hongchang Li, Yuan Gao, et al.
Prenatal Diagnosis
|
August 19, 2023
Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene
Yu Zheng, Lo Wong, Angel Hoi Wan Kwan, et al.
Genes
|
July 29, 2023
Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics
Keying Li, Yilin Zhao, Matthew Hoi Kin Chau, et al.
Current Protocols in Human Genetics
|
July 12, 2017
Copy-Number Variants Detection by Low-Pass Whole-Genome Sequencing
Zirui Dong, Weiwei Xie, Haixiao Chen, et al.
Journal of Advanced Research
|
August 10, 2025
Epigenetically silenced KAT2B suppresses de novo lipogenesis through destroying HDAC5/LSD1 complex assembly in renal cell carcinoma
Qi Wang, Daojia Miao, Ruijie Liu, et al.
Biomolecules
|
June 26, 2025
Gene Fusions as Potential Therapeutic Targets in Soft Tissue Sarcomas
Qiongdan Zheng, Tong Wang, Zijian Zou, et al.
Nature Communications
|
January 11, 2022
Half-Heusler-like compounds with wide continuous compositions and tunable p- to n-type semiconducting thermoelectrics
Zirui Dong, Jun Luo, Chenyang Wang, et al.
Prenatal Diagnosis
|
October 3, 2024
Contribution of Genomic Imbalance in Prenatal Congenital Anomalies of the Kidney and Urinary Tract: A Multi-Center Cohort Study
Keying Li, Huilin Wang, Matthew Hoi Kin Chau, et al.
Science China. Life Sciences
|
December 1, 2025
TEDD 2.0: an advanced temporal gene expression database enabled by in-silico functional analyses for developmental mechanism investigation
Chi Chun Chan, King Kin Lam, Lin Chen, et al.
Annals of Medicine
|
September 6, 2024
Detection of genomic variants by genome sequencing in foetuses with central nervous system abnormalities
Yanfei Wang, Meimei Liu, Zhi Gao, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 66) with videos related to
Sort By:
Page
of 7
Journal of Assisted Reproduction and Genetics
|
December 15, 2023
Identification of cryptic balanced translocations in couples with unexplained recurrent pregnancy loss based upon embryonic PGT-A results
Shuo Li, Hongchang Li, Yuan Gao, et al.
Prenatal Diagnosis
|
August 19, 2023
Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene
Yu Zheng, Lo Wong, Angel Hoi Wan Kwan, et al.
Genes
|
July 29, 2023
Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics
Keying Li, Yilin Zhao, Matthew Hoi Kin Chau, et al.
Current Protocols in Human Genetics
|
July 12, 2017
Copy-Number Variants Detection by Low-Pass Whole-Genome Sequencing
Zirui Dong, Weiwei Xie, Haixiao Chen, et al.
Journal of Advanced Research
|
August 10, 2025
Epigenetically silenced KAT2B suppresses de novo lipogenesis through destroying HDAC5/LSD1 complex assembly in renal cell carcinoma
Qi Wang, Daojia Miao, Ruijie Liu, et al.
Biomolecules
|
June 26, 2025
Gene Fusions as Potential Therapeutic Targets in Soft Tissue Sarcomas
Qiongdan Zheng, Tong Wang, Zijian Zou, et al.
Nature Communications
|
January 11, 2022
Half-Heusler-like compounds with wide continuous compositions and tunable p- to n-type semiconducting thermoelectrics
Zirui Dong, Jun Luo, Chenyang Wang, et al.
Prenatal Diagnosis
|
October 3, 2024
Contribution of Genomic Imbalance in Prenatal Congenital Anomalies of the Kidney and Urinary Tract: A Multi-Center Cohort Study
Keying Li, Huilin Wang, Matthew Hoi Kin Chau, et al.
Science China. Life Sciences
|
December 1, 2025
TEDD 2.0: an advanced temporal gene expression database enabled by in-silico functional analyses for developmental mechanism investigation
Chi Chun Chan, King Kin Lam, Lin Chen, et al.
Annals of Medicine
|
September 6, 2024
Detection of genomic variants by genome sequencing in foetuses with central nervous system abnormalities
Yanfei Wang, Meimei Liu, Zhi Gao, et al.
Page
of 7