Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Shi-Xiu Liao"'
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 55, Iss 6, Pp 867-870 (2016)
Objective: The aim of this report is to describe the phenotype-genotype correlation of chromosome 9p deletion syndrome cases, particularly the prenatal cases. Case report: We present a female fetus at 17+4 weeks of gestation age detected with an 8 ×
Externí odkaz:
https://doaj.org/article/59d0ef218e9f49458af6eb7c2560d5dd
Publikováno v:
BioMed Research International, Vol 2022 (2022)
BioMed Research International
BioMed Research International
Around the whole world, smoking is considered harmful to human health, such as increasing the risk of cardiovascular disease (CVD, such as coronary heart disease and stroke) and lung cancer. The purpose of this study was to explore whether nicotine,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2797a7f0f17288a4358aa685a9d8ad84
https://doi.org/10.1155/2022/4286621
https://doi.org/10.1155/2022/4286621
Publikováno v:
Reproductive biomedicine online. 45(6)
Do maternal homocysteine (Hcy) concentrations, MTHFR and MTRR genes have effects on the occurrence of fetal aneuploidy?A total of 619 aneuploidy mothers and 192 control mothers were recruited in this study. Differences in distributions of maternal MT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dee16ae15683eb3608932f9f04c55f8e
https://pubmed.ncbi.nlm.nih.gov/36210274
https://pubmed.ncbi.nlm.nih.gov/36210274
Autor:
Bofeng Zhu, Li Wang, Shi‑Xiu Liao, Qian‑Nan Guo, Lin Liu, Qiao‑Fang Hou, Jing‑Bin Yan, Hui‑Ru Zhao, Wei‑Li Shi, Hong‑Dan Wang
Publikováno v:
Molecular Medicine Reports
The discovery of cell-free DNA fetal (cff DNA) in maternal plasma during pregnancy provides a novel perspective for the development of non-invasive prenatal diagnosis (NIPD). Against the background of maternal DNA, the use of the relatively low conce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16c817e4727cc6739fedffa392750ed7
https://doi.org/10.3892/mmr.2017.6506
https://doi.org/10.3892/mmr.2017.6506
Autor:
Tao Li, Zhao-jing Zhang, Xin Ma, Xue Lv, Hai Xiao, Qian-nan Guo, Hong-yan Liu, Hong-dan Wang, Dong Wu, Gui-yu Lou, Xin Wang, Chao-yang Zhang, Shi-xiu Liao, Li, Tao, Zhang, Zhao-Jing, Ma, Xin, Lv, Xue, Xiao, Hai, Guo, Qian-Nan, Liu, Hong-Yan
Publikováno v:
Medicine; Dec2017, Vol. 96 Issue 50, p1-10, 10p
Autor:
HUI‑RU ZHAO, QIAO‑FANG HOU, WEI‑LI SHI, QIAN‑NAN GUO, LI WANG, SHI‑XIU LIAO, HONG‑DAN WANG, BO‑FENG ZHU, LIN LIU, JING‑BIN YAN
Publikováno v:
Molecular Medicine Reports; Jun2017, Vol. 15 Issue 6, p3989-3998, 10p, 6 Charts, 2 Graphs
Publikováno v:
Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology. 36(3)
We explored the strategies of prenatal diagnosis by foetal karyotype analysis in pregnant women with indications for genetic amniocentesis. Karyotype analysis of amniotic fluid was performed on 12365 pregnant women with indications for genetic amnioc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6b389488e060d0e3ce7c11b7cc74438
https://pubmed.ncbi.nlm.nih.gov/26445265
https://pubmed.ncbi.nlm.nih.gov/26445265
Analysis of etiology, chromosome and prognosis for small left heart system development in 69 fetuses
Autor:
Zhian Li, Lin Liu, Tao Li, Hui-mei Yao, Bangtian Peng, Shi-Xiu Liao, Taibing Fan, Lian-zhong Zhang, Cun-Ying Cui, Lei Huang, Yihua He
Objective: To provide a basis for evaluating the prognosis of small left heart system development in fetuses, we analyzed its related factors.Methods: The fetal echocardiogram was performed in 3859 pregnant women, and then small left heart system dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d1027f71e0b2f773a7071ac570d167c
Autor:
Ke, Yang, Bing, Zhang, Shu-xian, Cui, Qian-nan, Guo, Qiao-fang, Hou, Qian-cheng, Li, Shi-xiu, Liao
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 30(4)
To analyze CYP17A1 gene mutations in a child patient with 17 alpha-hydroxylase/17, 20-lyase deficiency (17OHD), and to review characteristics of CYP17A1 gene mutations in Chinese patients with 17OHD.Clinical data were collected. PCR and DNA sequencin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::90dd26ab1326cb97c7441fbe3398ff7f
https://pubmed.ncbi.nlm.nih.gov/23926012
https://pubmed.ncbi.nlm.nih.gov/23926012
Autor:
Yan, Chu, Dong, Fang, Qiao-fang, Hou, Li-ya, Wang, Xi-rang, Guo, Ying-tai, Wang, Shi-xiu, Liao
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 30(2)
To identify potential mutations of retinoschisis 1 (RS1) gene responsible for X-linked retinoschisis (XLRS) in two Chinese families.The 6 exons and flanking intronic regions were analyzed with PCR and direct sequencing.Two RS1 mutations were identifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d3db801cd66ac84d1ac36833ba3654a7
https://pubmed.ncbi.nlm.nih.gov/23568735
https://pubmed.ncbi.nlm.nih.gov/23568735