Central precocious puberty occurring in Bardet‑Biedl syndrome‑10 as a method for self‑protection of human reproductive function: A case report-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Central precocious puberty occurring in Bardet‑Biedl syndrome‑10 as a method for self‑protection of human reproductive function: A case report

Published:2022-07-15 Issue:3 Volume:24 Page:
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Li Hanming¹,He Jianyu¹,Leong Iatlun²,Huang Runxiao¹,Shi Xiaojie¹

Affiliation:

1. Department of Children's Health Care, Fifth People's Hospital of Foshan City, Foshan, Guangdong 528211, P.R. China

2. Department of General Surgery, University Hospital of Macau Special Administrative Region, Macau Special Administrative Region 999078, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

Reference30 articles.

1. On congenital obesity syndrome with polydactyly and retinitis pigmentosa (a contribution to the study of clinical forms of hypophyseal obesity);Bardet;Obes Res,1920

2. Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndrome;Ajmal;Mol Vis,2013

3. New criteria for improved diagnosis of Bardet-Biedl syndrome: Results of a population survey;Beales;J Med Genet,1999

4. Bardet-Biedl syndrome;Forsythe;Eur J Hum Genet,2013

5. Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: A 22-year prospective, population-based, cohort study;Moore;Am J Med Genet A,2005

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Review of the phenotypes and genotypes of Bardet-Biedl syndrome from China;Frontiers in Genetics;2023-11-15

2. Bardet-Biedl Syndrome: a case report of delayed diagnosis with variable presentation and role of genetic testing in definitive diagnosis;Egyptian Pediatric Association Gazette;2023-10-30

3. Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing;Human Genetics;2023-04-24

同舟云学术

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