Search research articles
Contact Us
Filters
Showing results (41-50 of 59) with videos related to
Page
of 6
Sort By:
Journal of Medical Genetics
|
November 13, 2025
Genetic and embryonic transcriptome analyses reveal the molecular and developmental basis of Mayer-Rokitansky-Küster-Hauser syndrome
Na Chen, Xi Cheng, Sen Zhao, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 24, 2025
Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosis
Lianlei Wang, Zhaoyang Liu, Sen Zhao, et al.
Nature Communications
|
February 6, 2024
Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine
Sen Zhao, Hengqiang Zhao, Lina Zhao, et al.
Journal of Human Genetics
|
August 18, 2018
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)
Kun Wang, Sen Zhao, Qianqian Zhang, et al.
Frontiers in Cell and Developmental Biology
|
May 3, 2021
Heterozygous Recurrent Mutations Inducing Dysfunction of <i>ROR2</i> Gene in Patients With Short Stature
Baoheng Gui, Chenxi Yu, Xiaoxin Li, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature
Xin Fan, Sen Zhao, Chenxi Yu, et al.
Journal of Human Genetics
|
December 13, 2019
Identification of novel FBN1 variations implicated in congenital scoliosis
Mao Lin, Sen Zhao, Gang Liu, et al.
Human Genetics
|
July 19, 2018
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease
Jiaqi Liu, Yangzhong Zhou, Sen Liu, et al.
Frontiers in Endocrinology
|
September 30, 2021
Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients
Chenxi Yu, Bobo Xie, Zhengye Zhao, et al.
Journal of Medical Genetics
|
August 19, 2018
Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)
Kun Wang, Sen Zhao, Bowen Liu, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 59) with videos related to
Sort By:
Page
of 6
Journal of Medical Genetics
|
November 13, 2025
Genetic and embryonic transcriptome analyses reveal the molecular and developmental basis of Mayer-Rokitansky-Küster-Hauser syndrome
Na Chen, Xi Cheng, Sen Zhao, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 24, 2025
Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosis
Lianlei Wang, Zhaoyang Liu, Sen Zhao, et al.
Nature Communications
|
February 6, 2024
Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine
Sen Zhao, Hengqiang Zhao, Lina Zhao, et al.
Journal of Human Genetics
|
August 18, 2018
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)
Kun Wang, Sen Zhao, Qianqian Zhang, et al.
Frontiers in Cell and Developmental Biology
|
May 3, 2021
Heterozygous Recurrent Mutations Inducing Dysfunction of <i>ROR2</i> Gene in Patients With Short Stature
Baoheng Gui, Chenxi Yu, Xiaoxin Li, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature
Xin Fan, Sen Zhao, Chenxi Yu, et al.
Journal of Human Genetics
|
December 13, 2019
Identification of novel FBN1 variations implicated in congenital scoliosis
Mao Lin, Sen Zhao, Gang Liu, et al.
Human Genetics
|
July 19, 2018
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease
Jiaqi Liu, Yangzhong Zhou, Sen Liu, et al.
Frontiers in Endocrinology
|
September 30, 2021
Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients
Chenxi Yu, Bobo Xie, Zhengye Zhao, et al.
Journal of Medical Genetics
|
August 19, 2018
Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)
Kun Wang, Sen Zhao, Bowen Liu, et al.
Page
of 6