Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Qiao-Fang Hou"'
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
Autor:
HUI‑RU ZHAO1, QIAO‑FANG HOU1, WEI‑LI SHI1, QIAN‑NAN GUO1, LI WANG1, SHI‑XIU LIAO1, HONG‑DAN WANG1,2, BO‑FENG ZHU2,3,4, LIN LIU5, JING‑BIN YAN5
Publikováno v:
Molecular Medicine Reports. Jun2017, Vol. 15 Issue 6, p3989-3998. 10p. 6 Charts, 2 Graphs.
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:
Hong-Dan Wang1,2 wanghongdan5495@163.com, Qiao-Fang Hou1 houqf_2000@163.com, Qian-Nan Guo1 guoqn1984@aliyun.com, Tao Li1 litao0510@163.com, Dong Wu1 wudong00@126.com, Xian-Ping Zhang3 zhangxianpingwj@126.com, Yan Chu1 chuyan1009@126.com, Miao He1 Michellehecat@126.com, Hai Xiao1 xiaohaizy@sina.com, Liang-Jie Guo1 guoliangjie@163.com, Ke Yang1 ykxiedi1986124@163.com, Shi-Xiu Liao1 syyliaoshixiu@163.com, Bo-Feng Zhu2 zhubofeng7372@126.com
Publikováno v:
BMC Medical Genomics. 2014, Vol. 7 Issue 1, p1-14. 14p.
Autor:
Shengbin Li, Qiao-Fang Hou
Publikováno v:
Neuroscience Letters. 464:127-130
The aim of our study was to investigate the potential association of dopamine receptor D2 gene (DRD2) TaqI RFLP A (rs1800497) and dopamine transporter gene (DAT) 3′untranslated region VNTR genetic variations with heroin addiction. Genotyping was pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68420dbc37697cc8bee6e35e1f70f558
https://doi.org/10.1016/j.neulet.2009.08.004
https://doi.org/10.1016/j.neulet.2009.08.004
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
Publikováno v:
Zhonghua fu chan ke za zhi. 48(2)
To assess the frequency and significance of maternal cell contamination (MCC) in the invasive prenatal diagnosis, and to analysis the MCC effect on prenatal diagnosis results.Totally 519 amniotic fluid samples from second trimester pregnancy, 57 chor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::95ca110123ee07314786b4bbed47e515
https://pubmed.ncbi.nlm.nih.gov/23544487
https://pubmed.ncbi.nlm.nih.gov/23544487
Autor:
Tao, Li, Dong, Wu, Qiao-fang, Hou, Li, Wang, Qian-nan, Guo, Bing, Kang, Hong-yan, Liu, Ke, Yang, Xue-bing, Ding, Shi-xiu, Liao
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 30(1)
To investigate the efficiency of multiplex ligation-dependent probe amplification (MLPA) combined with short tandem repeat (STR) linkage analysis for the prenatal diagnosis for Duchenne muscular dystrophy (DMD).Gender of the fetus was first determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b960e5fedaa5355a0a7e95ee7cd17351
https://pubmed.ncbi.nlm.nih.gov/23450477
https://pubmed.ncbi.nlm.nih.gov/23450477
Autor:
Qiao-fang, Hou, Dong, Wu, Yan, Chu, Bing, Kang, Shi-xiu, Liao, Yan-li, Yang, Chao-yang, Zhang, Ju-xin, Zhang, Gang, Wu
Publikováno v:
Zhonghua fu chan ke za zhi. 47(11)
To investigate the clinical value of non-invasive prenatal diagnosis using cell free fetal DNA (cff-DNA) in maternal blood.From Sep. 2010 to Mar. 2012, 103 pregnant women who came to Henan Province People's Hospital in the first trimester for prenata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ddf17524b4ccd852922a10d27cb44f89
https://pubmed.ncbi.nlm.nih.gov/23302120
https://pubmed.ncbi.nlm.nih.gov/23302120