Relationship between phenotype and genotype of 102 Chinese newborns with Prader–Willi syndrome-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Relationship between phenotype and genotype of 102 Chinese newborns with Prader–Willi syndrome

Published:2019-07-03 Issue:5 Volume:46 Page:4717-4724
ISSN:0301-4851
Container-title:Molecular Biology Reports
language:en
Short-container-title:Mol Biol Rep

Author:

Ge Meng-Meng,Gao Yan-Yan,Wu Bing-Bing,Yan Kai,Qin Qian,Wang HuiJun,Zhou WenHao,Yang Lin

Funder

Shanghai Health and Family Planning Commission Research Project

the National Key Research and Development Program of China

the Shanghai Municipal Commission of Health and Family Planning

the Shanghai Shen Kang Hospital Development Center

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s11033-019-04916-2.pdf

Reference32 articles.

1. Cassidy SB et al (2012) Prader–Willi syndrome. Genet Med 14(1):10–26

2. Crino A et al (2009) A survey on Prader–Willi syndrome in the Italian population: prevalence of historical and clinical signs. J Pediatr Endocrinol Metab 22(10):883–893

3. Holm VA et al (1993) Prader–Willi syndrome: consensus diagnostic criteria. Pediatrics 91(2):398–402

4. Shi F et al (2011) Infant brain atlases from neonates to 1- and 2-year-olds. PLoS ONE 6(4):e18746

5. Tabelow K et al (2011) Image analysis and statistical inference in neuroimaging with R. Neuroimage 55(4):1686–1693

Cited by 13 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. Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation;Frontiers in Endocrinology;2024-04-26

2. Neurodevelopmental Manifestations and Birth Defects in Prader-Willi Syndrome: Findings from a Study in Western Ukraine;Biomedical and Pharmacology Journal;2023-06-30

3. Progress in Brain Magnetic Resonance Imaging of Individuals with Prader–Willi Syndrome;Journal of Clinical Medicine;2023-01-29

4. Behavioral Phenotype of Patients with Prader-Willi Syndrome;Eating Disorders;2023

5. Facile discovery of red blood cell deformation and compromised membrane/skeleton assembly in Prader—Willi syndrome;Frontiers of Medicine;2022-11-17

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