Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Linjuan Su"'
Autor:
Xiaoqing Wu, Shengrong Du, Bin Liang, Linjuan Su, Ying Li, Yuqin Chen, Lin Zheng, Na Lin, Hailong Huang, Liangpu Xu
Publikováno v:
Heliyon, Vol 10, Iss 20, Pp e38387- (2024)
Prenatal diagnosis is crucial for pregnancies from couples with a carrier of a balanced translocation. We retrospectively reviewed 195 pregnancies from 189 couples with a balanced translocation carrier. Of these, 126 were from natural conception, whi
Externí odkaz:
https://doaj.org/article/19972505b32849248ae3414a1d0ffc0e
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-9 (2023)
Abstract Background With the advancement of molecular technology, fetal talipes equinovarus (TE) is believed to be not only associated with chromosome aneuploidy, but also related to chromosomal microdeletion and microduplication. The study aimed to
Externí odkaz:
https://doaj.org/article/76c783386d124ceba908327d2e2f70f0
Autor:
Meiying Cai, Na Lin, Nan Guo, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Ying Li, Shuqiong He, Xianguo Fu, Liangpu Xu, Hailong Huang
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract Numerous studies have evaluated the use of single nucleotide polymorphism array (SNP-array) in prenatal diagnostics, but very few have evaluated its application under different risk conditions. Here, SNP-array was used for the retrospective
Externí odkaz:
https://doaj.org/article/07b815492d184bcba9fdefbbbe30ede9
Autor:
Meiying Cai, Na Lin, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Shiyi Xu, Xianguo Fu, Liangpu Xu, Hailong Huang
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-9 (2022)
Abstract Background The etiology of fetal growth restriction (FGR) is complex and currently, there is a paucity of research about the genetic etiology of fetal growth restriction. We investigated the genetic associations and pregnancy outcomes in cas
Externí odkaz:
https://doaj.org/article/3a5fe9eb20c14bccb18f5f6ff7428aa7
Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios
Autor:
Xiaoqing Wu, Ying Li, Na Lin, Linjuan Su, Xiaorui Xie, Bing Liang, Qingmei Shen, Meiying Cai, Danhua Guo, Hailong Huang, Liangpu Xu
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-7 (2022)
Abstract Background Polyhydramnios, the excessive accumulation of amniotic fluid, is associated with an elevated risk of abnormal karyotype, particularly aneuploidy. Studies focusing on chromosomal microarray analysis (CMA) in pregnancies with polyhy
Externí odkaz:
https://doaj.org/article/557acb715f0041b18647a536ae21eea7
Autor:
Xiaoqing Wu, Linjuan Su, Xiaorui Xie, Deqin He, Xuemei Chen, Meiying Wang, Linshuo Wang, Lin Zheng, Liangpu Xu
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-8 (2021)
Abstract Background Pregnancy loss is one of the most common complications during pregnancy. Clinical consultation based on etiology analysis are critical for reducing anxiety and distress. This study aimed to perform a comprehensive analysis for pro
Externí odkaz:
https://doaj.org/article/439ef5e4e1514c69b17189d72c79ac58
Autor:
Xiaoqing Wu, Linjuan Su, Qingmei Shen, Qun Guo, Ying Li, Shiyi Xu, Na Lin, Hailong Huang, Liangpu Xu
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Externí odkaz:
https://doaj.org/article/aeaf9e15927b41eb86aaeba771a9b268
Autor:
Xiaoqing Wu, Linjuan Su, Qingmei Shen, Qun Guo, Ying Li, Shiyi Xu, Na Lin, Hailong Huang, Liangpu Xu
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Fetal gastrointestinal tract obstruction (GITO) is the most frequently encountered gastrointestinal defect in the prenatal period. This study aimed to investigate the genetic disorders and pregnancy outcomes of fetal GITO. We reviewed data from 70 pr
Externí odkaz:
https://doaj.org/article/ad032456cf3742d8a2da6b727cd80f89
Autor:
Meiying Cai, Na Lin, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Ying Li, Xuemei Chen, Yuan Lin, Hailong Huang, Liangpu Xu
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-6 (2020)
Abstract Background Congenital anomalies of the kidney and urinary tract (CAKUT) constitute 20–30% of all congenital malformations. Within the CAKUT phenotypic spectrum, renal hypodysplasia (RHD) is particularly severe. This study aimed to evaluate
Externí odkaz:
https://doaj.org/article/c8243580e11c47288a4fde67ffec63d9
Autor:
Xiaoqing Wu, Liangpu Xu, Ying Li, Na Lin, Linjuan Su, Meiying Cai, Xiaorui Xie, Lin Zheng, Hailong Huang, Yuan Lin
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-7 (2019)
Abstract Background Nearly 9.89% of chromosome 16 consists of segmental duplications, which makes it prone to non-homologous recombination. The present study aimed to investigate the incidence and perinatal characteristics of submicroscopic chromosom
Externí odkaz:
https://doaj.org/article/5033a2dd7bc1491298b95f89ee038fa6