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Shanling Liu

Showing results (111-120 of 175) with videos related to

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Scientific Reports|November 28, 2020
Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in foetuses with ventriculomegalyJiamin Wang, Zhu Zhang, Qinqin Li, et al.
Frontiers in Genetics|June 20, 2022
Case Report: Preimplantation Genetic Testing for X-Linked Severe Combined Immune Deficiency Caused by <i>IL2RG</i> Gene VariantJun Ren, Cuiting Peng, Fan Zhou, et al.
Prenatal Diagnosis|June 26, 2020
Comparison of spontaneous fetal loss rates between women with singleton and twin pregnancies after mid-trimester amniocentesis - A historical cohort studyJiawei Chen, Linhu Liu, Dan Xia, et al.
Prenatal Diagnosis|January 11, 2024
Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three casesXijing Liu, Zhu Zhang, Xuan Zhang, et al.
Molecular Genetics & Genomic Medicine|June 14, 2025
A Novel Synonymous Variant of PAX2 in Monochorionic Diamniotic Twins With Bilateral Renal Agenesis: A Case Report and Literature ReviewWencong Yao, Bocheng Xu, Hao Wang, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|March 19, 2025
Prenatal manifestations of 3q29 deletion: A potential relationship with enlarged nuchal translucencyXijing Liu, Jiamin Wang, Rui Hu, et al.
Clinical Genetics|January 15, 2024
Functional characterization of inactivating ABCC8 variants causing congenital hyperinsulinismPing Wang, Hong Liao, Quyou Wang, et al.
Diagnostic Pathology|January 23, 2014
Expression of serum amyloid A in uterine cervical cancerYanjie Ren, He Wang, Donghao Lu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 9, 2022
[Application of copy number variation squencing for prenatal diagnosis]Quyou Wang, Ting Hu, Lin Chen, et al.
Journal of Endocrinological Investigation|May 7, 2026
From genetic diagnosis to healthy live births: implementing an integrated PGT-M pathway for 21-hydroxylase deficiencyXinlian Chen, Cuiting Peng, Han Chen, et al.
Pageof 18

Showing results (111-120 of 175) with videos related to

Sort By:
Pageof 18
Scientific Reports|November 28, 2020
Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in foetuses with ventriculomegalyJiamin Wang, Zhu Zhang, Qinqin Li, et al.
Frontiers in Genetics|June 20, 2022
Case Report: Preimplantation Genetic Testing for X-Linked Severe Combined Immune Deficiency Caused by <i>IL2RG</i> Gene VariantJun Ren, Cuiting Peng, Fan Zhou, et al.
Prenatal Diagnosis|June 26, 2020
Comparison of spontaneous fetal loss rates between women with singleton and twin pregnancies after mid-trimester amniocentesis - A historical cohort studyJiawei Chen, Linhu Liu, Dan Xia, et al.
Prenatal Diagnosis|January 11, 2024
Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three casesXijing Liu, Zhu Zhang, Xuan Zhang, et al.
Molecular Genetics & Genomic Medicine|June 14, 2025
A Novel Synonymous Variant of PAX2 in Monochorionic Diamniotic Twins With Bilateral Renal Agenesis: A Case Report and Literature ReviewWencong Yao, Bocheng Xu, Hao Wang, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|March 19, 2025
Prenatal manifestations of 3q29 deletion: A potential relationship with enlarged nuchal translucencyXijing Liu, Jiamin Wang, Rui Hu, et al.
Clinical Genetics|January 15, 2024
Functional characterization of inactivating ABCC8 variants causing congenital hyperinsulinismPing Wang, Hong Liao, Quyou Wang, et al.
Diagnostic Pathology|January 23, 2014
Expression of serum amyloid A in uterine cervical cancerYanjie Ren, He Wang, Donghao Lu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 9, 2022
[Application of copy number variation squencing for prenatal diagnosis]Quyou Wang, Ting Hu, Lin Chen, et al.
Journal of Endocrinological Investigation|May 7, 2026
From genetic diagnosis to healthy live births: implementing an integrated PGT-M pathway for 21-hydroxylase deficiencyXinlian Chen, Cuiting Peng, Han Chen, et al.
Pageof 18