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Linjuan Su

Showing results (31-40 of 39) with videos related to

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Heliyon|November 5, 2024
Single Nucleotide Polymorphism array analysis for fetuses from balanced translocation carriers at the second trimesterXiaoqing Wu, Shengrong Du, Bin Liang, et al.
Molecular Cytogenetics|December 7, 2018
Chromosomal abnormalities and copy number variations in fetal ventricular septal defectsMeiying Cai, Hailong Huang, Linjuan Su, et al.
BMC Medical Genomics|March 31, 2022
Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramniosXiaoqing Wu, Ying Li, Na Lin, et al.
Gene|November 17, 2023
Genetic evaluation for twin pregnancies using karyotyping and single nucleotide polymorphism array analysisXiaoqing Wu, Baojia Huang, Xiaorui Xie, et al.
Scientific Reports|May 4, 2023
Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern ChinaMeiying Cai, Na Lin, Nan Guo, et al.
Journal of Clinical Laboratory Analysis|September 12, 2019
Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arraysMeiying Cai, Na Lin, Linjuan Su, et al.
Journal of Cellular and Molecular Medicine|May 27, 2021
Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testingXiaoqing Wu, Ying Li, Na Lin, et al.
Journal of Perinatal Medicine|May 4, 2023
Prenatal diagnosis of non-mosaic sex chromosome abnormalities: a 10-year experience from a tertiary referral centerXiaoqing Wu, Danhua Guo, Ying Li, et al.
Journal of Clinical Laboratory Analysis|November 26, 2019
Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal ageXiaoqing Wu, Gang An, Xiaorui Xie, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Heliyon|November 5, 2024
Single Nucleotide Polymorphism array analysis for fetuses from balanced translocation carriers at the second trimesterXiaoqing Wu, Shengrong Du, Bin Liang, et al.
Molecular Cytogenetics|December 7, 2018
Chromosomal abnormalities and copy number variations in fetal ventricular septal defectsMeiying Cai, Hailong Huang, Linjuan Su, et al.
BMC Medical Genomics|March 31, 2022
Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramniosXiaoqing Wu, Ying Li, Na Lin, et al.
Gene|November 17, 2023
Genetic evaluation for twin pregnancies using karyotyping and single nucleotide polymorphism array analysisXiaoqing Wu, Baojia Huang, Xiaorui Xie, et al.
Scientific Reports|May 4, 2023
Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern ChinaMeiying Cai, Na Lin, Nan Guo, et al.
Journal of Clinical Laboratory Analysis|September 12, 2019
Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arraysMeiying Cai, Na Lin, Linjuan Su, et al.
Journal of Cellular and Molecular Medicine|May 27, 2021
Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testingXiaoqing Wu, Ying Li, Na Lin, et al.
Journal of Perinatal Medicine|May 4, 2023
Prenatal diagnosis of non-mosaic sex chromosome abnormalities: a 10-year experience from a tertiary referral centerXiaoqing Wu, Danhua Guo, Ying Li, et al.
Journal of Clinical Laboratory Analysis|November 26, 2019
Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal ageXiaoqing Wu, Gang An, Xiaorui Xie, et al.
Pageof 4