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

Saved in:
Bibliographic Details
Published in:Annals of dermatology 2019, Vol.31 (s4), p.10
Main Authors: Emin Ozlu, Ayse Serap Karadag, Ibrahim Akalın, Gozde Yesil, Sarenur Yılmaz, Ilkin Zindancı, Tugba Kevser Uzuncakmak, Seyma Ozkanlı, Necmettin Akdeniz
Format: Article
Language:Korean
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page
container_issue s4
container_start_page 10
container_title Annals of dermatology
container_volume 31
creator Emin Ozlu
Ayse Serap Karadag
Ibrahim Akalın
Gozde Yesil
Sarenur Yılmaz
Ilkin Zindancı
Tugba Kevser Uzuncakmak
Seyma Ozkanlı
Necmettin Akdeniz
description
format article
fullrecord <record><control><sourceid>kiss</sourceid><recordid>TN_cdi_kiss_primary_3689998</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><kiss_id>3689998</kiss_id><sourcerecordid>3689998</sourcerecordid><originalsourceid>FETCH-kiss_primary_36899983</originalsourceid><addsrcrecordid>eNp9jE8LwiAcQCUKsj-foMvvCwg6a9NjRK1LMVj3IWRkOQ21Yn36dujc6T148AYIZ5SuCBdyOUSYUcaJpKIYo0mMN0pzlhUMo_XRv7SF6rTZMyi103B4JpWMd2AcKKh61y7B26QrlD5Y40jpbfpA3blz8K2eodFF2ajnP07RYrftd-RuYmwewbQqdA3PhZRS8P_1Cx8uM-s</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome</title><source>PubMed Central</source><creator>Emin Ozlu ; Ayse Serap Karadag ; Ibrahim Akalın ; Gozde Yesil ; Sarenur Yılmaz ; Ilkin Zindancı ; Tugba Kevser Uzuncakmak ; Seyma Ozkanlı ; Necmettin Akdeniz</creator><creatorcontrib>Emin Ozlu ; Ayse Serap Karadag ; Ibrahim Akalın ; Gozde Yesil ; Sarenur Yılmaz ; Ilkin Zindancı ; Tugba Kevser Uzuncakmak ; Seyma Ozkanlı ; Necmettin Akdeniz</creatorcontrib><identifier>ISSN: 1013-9087</identifier><identifier>EISSN: 2005-3894</identifier><language>kor</language><publisher>대한피부과학회</publisher><ispartof>Annals of dermatology, 2019, Vol.31 (s4), p.10</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024</link.rule.ids></links><search><creatorcontrib>Emin Ozlu</creatorcontrib><creatorcontrib>Ayse Serap Karadag</creatorcontrib><creatorcontrib>Ibrahim Akalın</creatorcontrib><creatorcontrib>Gozde Yesil</creatorcontrib><creatorcontrib>Sarenur Yılmaz</creatorcontrib><creatorcontrib>Ilkin Zindancı</creatorcontrib><creatorcontrib>Tugba Kevser Uzuncakmak</creatorcontrib><creatorcontrib>Seyma Ozkanlı</creatorcontrib><creatorcontrib>Necmettin Akdeniz</creatorcontrib><title>Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome</title><title>Annals of dermatology</title><addtitle>Annals of Dermatology</addtitle><issn>1013-9087</issn><issn>2005-3894</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9jE8LwiAcQCUKsj-foMvvCwg6a9NjRK1LMVj3IWRkOQ21Yn36dujc6T148AYIZ5SuCBdyOUSYUcaJpKIYo0mMN0pzlhUMo_XRv7SF6rTZMyi103B4JpWMd2AcKKh61y7B26QrlD5Y40jpbfpA3blz8K2eodFF2ajnP07RYrftd-RuYmwewbQqdA3PhZRS8P_1Cx8uM-s</recordid><startdate>2019</startdate><enddate>2019</enddate><creator>Emin Ozlu</creator><creator>Ayse Serap Karadag</creator><creator>Ibrahim Akalın</creator><creator>Gozde Yesil</creator><creator>Sarenur Yılmaz</creator><creator>Ilkin Zindancı</creator><creator>Tugba Kevser Uzuncakmak</creator><creator>Seyma Ozkanlı</creator><creator>Necmettin Akdeniz</creator><general>대한피부과학회</general><scope>HZB</scope><scope>Q5X</scope></search><sort><creationdate>2019</creationdate><title>Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome</title><author>Emin Ozlu ; Ayse Serap Karadag ; Ibrahim Akalın ; Gozde Yesil ; Sarenur Yılmaz ; Ilkin Zindancı ; Tugba Kevser Uzuncakmak ; Seyma Ozkanlı ; Necmettin Akdeniz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kiss_primary_36899983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2019</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Emin Ozlu</creatorcontrib><creatorcontrib>Ayse Serap Karadag</creatorcontrib><creatorcontrib>Ibrahim Akalın</creatorcontrib><creatorcontrib>Gozde Yesil</creatorcontrib><creatorcontrib>Sarenur Yılmaz</creatorcontrib><creatorcontrib>Ilkin Zindancı</creatorcontrib><creatorcontrib>Tugba Kevser Uzuncakmak</creatorcontrib><creatorcontrib>Seyma Ozkanlı</creatorcontrib><creatorcontrib>Necmettin Akdeniz</creatorcontrib><collection>KISS</collection><collection>Korean Studies Information Service System (KISS) B-Type</collection><jtitle>Annals of dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Emin Ozlu</au><au>Ayse Serap Karadag</au><au>Ibrahim Akalın</au><au>Gozde Yesil</au><au>Sarenur Yılmaz</au><au>Ilkin Zindancı</au><au>Tugba Kevser Uzuncakmak</au><au>Seyma Ozkanlı</au><au>Necmettin Akdeniz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome</atitle><jtitle>Annals of dermatology</jtitle><addtitle>Annals of Dermatology</addtitle><date>2019</date><risdate>2019</risdate><volume>31</volume><issue>s4</issue><spage>10</spage><pages>10-</pages><issn>1013-9087</issn><eissn>2005-3894</eissn><pub>대한피부과학회</pub><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1013-9087
ispartof Annals of dermatology, 2019, Vol.31 (s4), p.10
issn 1013-9087
2005-3894
language kor
recordid cdi_kiss_primary_3689998
source PubMed Central
title Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T02%3A24%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-kiss&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Novel%20PTCH1%20Gene%20Mutation%20in%20a%20Patient%20with%20Gorlin-Goltz%20Syndrome&rft.jtitle=Annals%20of%20dermatology&rft.au=Emin%20Ozlu&rft.date=2019&rft.volume=31&rft.issue=s4&rft.spage=10&rft.pages=10-&rft.issn=1013-9087&rft.eissn=2005-3894&rft_id=info:doi/&rft_dat=%3Ckiss%3E3689998%3C/kiss%3E%3Cgrp_id%3Ecdi_FETCH-kiss_primary_36899983%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rft_kiss_id=3689998&rfr_iscdi=true