Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Shaobin Lin

Showing results (51-60 of 92) with videos related to

Pageof 10
Sort By:
Molecular Cytogenetics|May 19, 2021
Mosaic duplication of 8q24.1q24.3 detected by chromosomal microarray but not karyotyping in two unrelated fetuses with cardiac defectsShaobin Lin, Shufang Huang, Xueling Ou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 4, 2020
[A consensus recommendation for the interpretation and reporting of copy number variation and regions of homozygosity in prenatal genetic diagnosis]Weiqiang Liu, Jian Lu, Jun Zhang, et al.
Scientific Reports|April 14, 2025
Retrospective study on NIPT or NIPT plus combined with ultrasound in screening fetal chromosomal abnormalitiesMeilin Chen, Peisong Chen, Siyang Yu, et al.
Prenatal Diagnosis|November 25, 2017
Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasiaZhiyong Zou, Linhuan Huang, Shaobin Lin, et al.
Electrophoresis|July 16, 2023
Application of SNPs with low minor allele frequencies in missing person identification (MPI) through kinship analysis of DNA mixturesNan Zhang, Shanshan Shi, Shaobin Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 22, 2020
[Clinical and genetic analysis of a patient with 17-hydroxylase/17,20-lyase deficiency]Yu Zeng, Libin Mei, Lei Liang, et al.
Prenatal Diagnosis|May 26, 2016
Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restrictionHui Zhu, Shaobin Lin, Linhuan Huang, et al.
Prenatal Diagnosis|March 8, 2018
Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletionsShaobin Lin, Shanshan Shi, Yi Zhou, et al.
Molecular Cytogenetics|July 18, 2019
Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?Shaobin Lin, Shanshan Shi, Linhuan Huang, et al.
Italian Journal of Pediatrics|July 1, 2020
A child with a novel DDX3X variant mimicking cerebral palsy: a case reportLiqin Hu, Xiaoqin Xin, Shaobin Lin, et al.
Pageof 10

Showing results (51-60 of 92) with videos related to

Sort By:
Pageof 10
Molecular Cytogenetics|May 19, 2021
Mosaic duplication of 8q24.1q24.3 detected by chromosomal microarray but not karyotyping in two unrelated fetuses with cardiac defectsShaobin Lin, Shufang Huang, Xueling Ou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 4, 2020
[A consensus recommendation for the interpretation and reporting of copy number variation and regions of homozygosity in prenatal genetic diagnosis]Weiqiang Liu, Jian Lu, Jun Zhang, et al.
Scientific Reports|April 14, 2025
Retrospective study on NIPT or NIPT plus combined with ultrasound in screening fetal chromosomal abnormalitiesMeilin Chen, Peisong Chen, Siyang Yu, et al.
Prenatal Diagnosis|November 25, 2017
Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasiaZhiyong Zou, Linhuan Huang, Shaobin Lin, et al.
Electrophoresis|July 16, 2023
Application of SNPs with low minor allele frequencies in missing person identification (MPI) through kinship analysis of DNA mixturesNan Zhang, Shanshan Shi, Shaobin Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 22, 2020
[Clinical and genetic analysis of a patient with 17-hydroxylase/17,20-lyase deficiency]Yu Zeng, Libin Mei, Lei Liang, et al.
Prenatal Diagnosis|May 26, 2016
Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restrictionHui Zhu, Shaobin Lin, Linhuan Huang, et al.
Prenatal Diagnosis|March 8, 2018
Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletionsShaobin Lin, Shanshan Shi, Yi Zhou, et al.
Molecular Cytogenetics|July 18, 2019
Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?Shaobin Lin, Shanshan Shi, Linhuan Huang, et al.
Italian Journal of Pediatrics|July 1, 2020
A child with a novel DDX3X variant mimicking cerebral palsy: a case reportLiqin Hu, Xiaoqin Xin, Shaobin Lin, et al.
Pageof 10