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Scientific Reports
|
May 4, 2023
Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China
Meiying 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 arrays
Meiying Cai, Na Lin, Linjuan Su, et al.
Molecular Cytogenetics
|
December 7, 2018
Chromosomal abnormalities and copy number variations in fetal ventricular septal defects
Meiying Cai, Hailong Huang, 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 testing
Xiaoqing 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 center
Xiaoqing Wu, Danhua Guo, Ying Li, et al.
BMC Pregnancy and Childbirth
|
September 19, 2023
Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study
Yanting Que, Meiying Cai, Fang Yang, et al.
Laboratory Medicine
|
September 2, 2022
Application of the Single-Molecule Real-Time Technology (SMRT) for Identification of HKαα Thalassemia Allele
Min Zhang, Zhaodong Lin, Meihuan Chen, 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 age
Xiaoqing Wu, Gang An, Xiaorui Xie, et al.
Frontiers in Pediatrics
|
May 2, 2025
Incidental finding of a <i>DMD</i> exons 48-55 deletion during prenatal diagnosis
Min Zhang, Zhaodong Lin, Meihuan Chen, et al.
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Search research articles
Search
Showing results (71-80 of 79) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 79 results.
Scientific Reports
|
May 4, 2023
Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China
Meiying 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 arrays
Meiying Cai, Na Lin, Linjuan Su, et al.
Molecular Cytogenetics
|
December 7, 2018
Chromosomal abnormalities and copy number variations in fetal ventricular septal defects
Meiying Cai, Hailong Huang, 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 testing
Xiaoqing 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 center
Xiaoqing Wu, Danhua Guo, Ying Li, et al.
BMC Pregnancy and Childbirth
|
September 19, 2023
Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study
Yanting Que, Meiying Cai, Fang Yang, et al.
Laboratory Medicine
|
September 2, 2022
Application of the Single-Molecule Real-Time Technology (SMRT) for Identification of HKαα Thalassemia Allele
Min Zhang, Zhaodong Lin, Meihuan Chen, 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 age
Xiaoqing Wu, Gang An, Xiaorui Xie, et al.
Frontiers in Pediatrics
|
May 2, 2025
Incidental finding of a <i>DMD</i> exons 48-55 deletion during prenatal diagnosis
Min Zhang, Zhaodong Lin, Meihuan Chen, et al.
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of 8