Copy Number Variation Analysis in Turkish Patients with Congenital Bilateral Absence of Vas Deferens
Author:
Publisher
Acta Medica Alanya
Reference39 articles.
1. Kumar N, Singh AK. Trends of male factor infertility, an important cause of infertility: A review of literature. J Hum Reprod Sci. 2015;8(4):191-6. doi: 10.4103/0974-1208.170370.
2. Lidegaard O, Mikkelsen AL, Meldgaard M, Brondum-Nielsen K, Lindenberg S. Severe male infertility. Impact of genetic factors on diagnosis and counselling. Acta Obstet Gynecol Scand. 1998;77(8):799-803.
3. Lee CH, Wu CC, Wu YN, Chiang HS. Gene copy number variations in Asian patients with congenital bilateral absence of the vas deferens. Human reproduction. 2009;24(3):748-55. doi: 10.1093/humrep/den413.
4. Yu J, Chen Z, Ni Y, Li Z. CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis. Human reproduction. 2012;27(1):25-35. doi: 10.1093/humrep/der377.
5. Ocak Z, Uyetuork U, Dincer MM. Clinical and prognostic importance of chromosomal abnormalities, Y chromosome microdeletions, and CFTR gene mutations in individuals with azoospermia or severe oligospermia. Turkish journal of medical sciences. 2014;44(2):347-51.
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3