Search research articles
Contact Us
Filters
Showing results (21-30 of 36) with videos related to
Page
of 4
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 29, 2020
Single nucleotide polymorphism array analysis of 102 patients with developmental delay and/or intellectual disability from Fujian, China
Bin Liang, Yan Wang, Na Lin, et al.
The Journal of Molecular Diagnostics : JMD
|
August 29, 2020
The Comprehensive Comparison of Bacterial Artificial Chromosomes (BACs)-on-Beads Assay and Copy Number Variation Sequencing in Prenatal Diagnosis of Southern Chinese Women
LiangPu Xu, Min Zhang, HaiLong Huang, et al.
Scientific Reports
|
March 7, 2019
Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China
Hailong Huang, Liangpu Xu, Meihuan Chen, et al.
Molecular Genetics and Genomics : MGG
|
July 28, 2022
Application of the prenatal BACs-on-Beads™ assay for rapid prenatal detection of sex chromosome mosaicism
Min Zhang, LingJi Chen, Meihuan Chen, et al.
Journal of Clinical Laboratory Analysis
|
January 17, 2020
X-linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations
Min Zhang, Hailong Huang, Na Lin, et al.
Scientific Reports
|
January 25, 2024
Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing
Huili Xue, Aili Yu, Lin Zhang, et al.
Frontiers in Neuroscience
|
May 30, 2023
Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy
Bin Mao, Na Lin, Danhua Guo, et al.
Scientific Reports
|
July 2, 2025
Prenatally and postnatally sequential genetic etiology detection in corpus callosum abnormalities
Huili Xue, Aili Yu, Lin Zheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 6, 2019
[Variant analysis for patients from Fujian area with Hong Kong αα type thalassemia]
Min Zhang, Hailong Huang, Meihuan Chen, et al.
Scientific Reports
|
November 9, 2024
Prenatal diagnosis of fetal skeletal anomalies via whole-exome sequencing in a tertiary referral center
Huili Xue, Aili Yu, Wantong Zhao, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 36) with videos related to
Sort By:
Page
of 4
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 29, 2020
Single nucleotide polymorphism array analysis of 102 patients with developmental delay and/or intellectual disability from Fujian, China
Bin Liang, Yan Wang, Na Lin, et al.
The Journal of Molecular Diagnostics : JMD
|
August 29, 2020
The Comprehensive Comparison of Bacterial Artificial Chromosomes (BACs)-on-Beads Assay and Copy Number Variation Sequencing in Prenatal Diagnosis of Southern Chinese Women
LiangPu Xu, Min Zhang, HaiLong Huang, et al.
Scientific Reports
|
March 7, 2019
Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China
Hailong Huang, Liangpu Xu, Meihuan Chen, et al.
Molecular Genetics and Genomics : MGG
|
July 28, 2022
Application of the prenatal BACs-on-Beads™ assay for rapid prenatal detection of sex chromosome mosaicism
Min Zhang, LingJi Chen, Meihuan Chen, et al.
Journal of Clinical Laboratory Analysis
|
January 17, 2020
X-linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations
Min Zhang, Hailong Huang, Na Lin, et al.
Scientific Reports
|
January 25, 2024
Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing
Huili Xue, Aili Yu, Lin Zhang, et al.
Frontiers in Neuroscience
|
May 30, 2023
Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy
Bin Mao, Na Lin, Danhua Guo, et al.
Scientific Reports
|
July 2, 2025
Prenatally and postnatally sequential genetic etiology detection in corpus callosum abnormalities
Huili Xue, Aili Yu, Lin Zheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 6, 2019
[Variant analysis for patients from Fujian area with Hong Kong αα type thalassemia]
Min Zhang, Hailong Huang, Meihuan Chen, et al.
Scientific Reports
|
November 9, 2024
Prenatal diagnosis of fetal skeletal anomalies via whole-exome sequencing in a tertiary referral center
Huili Xue, Aili Yu, Wantong Zhao, et al.
Page
of 4