Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome

Published:2019 Issue:Suppl Volume:31 Page:S10
ISSN:1013-9087
Container-title:Annals of Dermatology
language:en
Short-container-title:Ann Dermatol

Author:

Ozlu Emin¹^ORCID,Karadag Ayse Serap²^ORCID,Akalın Ibrahim³^ORCID,Yesil Gozde³^ORCID,Yılmaz Sarenur⁴^ORCID,Zindancı Ilkin²^ORCID,Uzuncakmak Tugba Kevser²^ORCID,Ozkanlı Seyma⁵^ORCID,Akdeniz Necmettin²^ORCID

Affiliation:

1. Department of Dermatology, Duzce University, Duzce, Turkey.

2. Department of Dermatology, Istanbul Medeniyet University School of Medicine, Istanbul, Turkey.

3. Department of Medical Genetics, Istanbul Medeniyet University School of Medicine, Istanbul, Turkey.

4. Department of Medical Genetics, Bezmialem University School of Medicine, Istanbul, Turkey.

5. Department of Pathology, Istanbul Medeniyet University School of Medicine, Istanbul, Turkey.

Publisher

Korean Dermatological Association and The Korean Society for Investigative Dermatology

Subject

Dermatology

Link

https://synapse.koreamed.org/pdf/10.5021/ad.2019.31.S.S10

Cited by 2 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. Nevoid Basal Cell Carcinoma Syndrome on Scalp: A Rare Case Report;Korean Society for Head and Neck Oncology;2023-11-30

2. Radiological evaluation of odontogenic keratocysts in patients with nevoid basal cell carcinoma syndrome: A review;The Saudi Dental Journal;2023-09

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