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

Linjuan Su

Showing results (21-30 of 39) with videos related to

Pageof 4
Sort By:
Scientific Reports|September 16, 2020
Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypesMeiying Cai, Na Lin, Linjuan Su, et al.
Journal of Cellular and Molecular Medicine|August 18, 2021
Prenatal diagnosis of Pallister-Killian syndrome and literature reviewXiaoqing Wu, Xiaorui Xie, Linjuan Su, et al.
The Journal of Molecular Diagnostics : JMD|October 18, 2020
Clinical Review of Noninvasive Prenatal Testing: Experience from 551 Pregnancies with Noninvasive Prenatal Testing-Positive Results in a Tertiary Referral CenterXiaoqing Wu, Ying Li, Xiaorui Xie, et al.
Molecular Cytogenetics|December 5, 2021
Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral centerXiaoqing Wu, Linjuan Su, Xiaorui Xie, et al.
Frontiers in Pediatrics|November 17, 2022
Corrigendum: Chromosomal abnormalities and pregnancy outcomes for fetuses with gastrointestinal tract obstructionsXiaoqing Wu, Linjuan Su, Qingmei Shen, et al.
Medicine|December 19, 2018
Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcomeMeiying Cai, Hailong Huang, Linjuan Su, et al.
Molecular Genetics & Genomic Medicine|June 19, 2019
Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotypeLinjuan Su, Hailong Huang, Gang An, et al.
Molecular Cytogenetics|March 27, 2020
Copy number variations associated with fetal congenital kidney malformationsMeiying Cai, Na Lin, Linjuan Su, et al.
Molecular Cytogenetics|August 9, 2019
Submicroscopic aberrations of chromosome 16 in prenatal diagnosisXiaoqing Wu, Liangpu Xu, Ying Li, et al.
Molecular Biology Reports|August 5, 2025
Prenatal genetic findings using karyotyping and chromosomal microarray analysis in the first-occurrence typical orofacial cleftsXiaoqing Wu, Xiaorui Xie, Jinzhou Lu, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Scientific Reports|September 16, 2020
Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypesMeiying Cai, Na Lin, Linjuan Su, et al.
Journal of Cellular and Molecular Medicine|August 18, 2021
Prenatal diagnosis of Pallister-Killian syndrome and literature reviewXiaoqing Wu, Xiaorui Xie, Linjuan Su, et al.
The Journal of Molecular Diagnostics : JMD|October 18, 2020
Clinical Review of Noninvasive Prenatal Testing: Experience from 551 Pregnancies with Noninvasive Prenatal Testing-Positive Results in a Tertiary Referral CenterXiaoqing Wu, Ying Li, Xiaorui Xie, et al.
Molecular Cytogenetics|December 5, 2021
Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral centerXiaoqing Wu, Linjuan Su, Xiaorui Xie, et al.
Frontiers in Pediatrics|November 17, 2022
Corrigendum: Chromosomal abnormalities and pregnancy outcomes for fetuses with gastrointestinal tract obstructionsXiaoqing Wu, Linjuan Su, Qingmei Shen, et al.
Medicine|December 19, 2018
Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcomeMeiying Cai, Hailong Huang, Linjuan Su, et al.
Molecular Genetics & Genomic Medicine|June 19, 2019
Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotypeLinjuan Su, Hailong Huang, Gang An, et al.
Molecular Cytogenetics|March 27, 2020
Copy number variations associated with fetal congenital kidney malformationsMeiying Cai, Na Lin, Linjuan Su, et al.
Molecular Cytogenetics|August 9, 2019
Submicroscopic aberrations of chromosome 16 in prenatal diagnosisXiaoqing Wu, Liangpu Xu, Ying Li, et al.
Molecular Biology Reports|August 5, 2025
Prenatal genetic findings using karyotyping and chromosomal microarray analysis in the first-occurrence typical orofacial cleftsXiaoqing Wu, Xiaorui Xie, Jinzhou Lu, et al.
Pageof 4