GLI3 mutations in syndromic and non-syndromic polydactyly in two Indian families

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Congenital Anomalies 2016, Vol.56 (2), p.94-97
Hauptverfasser:	Patel, Rashmi, Singh, Chandra Bhan, Bhattacharya, Visweswar, Singh, Subodh Kumar, Ali, Akhtar
Format:	Report
Sprache:	eng
Schlagworte:	Greig Cephalopolysyndactyly Syndrome India limb defects mutation polydactyly
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

container_end_page	97
container_issue	2
container_start_page	94
container_title	Congenital Anomalies
container_volume	56
creator	Patel, Rashmi Singh, Chandra Bhan Bhattacharya, Visweswar Singh, Subodh Kumar Ali, Akhtar
description
doi_str_mv	10.1111/cga.12139
format	Report
fullrecord	<record><control><sourceid>istex</sourceid><recordid>TN_cdi_istex_primary_ark_67375_WNG_T297SJ15_T</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_T297SJ15_T</sourcerecordid><originalsourceid>FETCH-istex_primary_ark_67375_WNG_T297SJ15_T3</originalsourceid><addsrcrecordid>eNqVis2KwjAYAIO4YHX34BvkBeImTdPQs2h1EREseAwf_VmibVKaiObtdwXBs3MZGAahOaML9s93-QsLFjOejVDEZMJIImI6RhHNWEK4oGKCps6dKY3TVNIIHfLdluPu6sFraxzWBrtgqsF2usRgKmysIa_S2zZUUPrQhsfqbxZvTaXB4AY63erafaKPBlpXfz09Q2S9KpYbop2v76ofdAdDUDBcVCq5FOq0z1URZ_L4w4Qq-Lv_H20BSrw</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>report</recordtype></control><display><type>report</type><title>GLI3 mutations in syndromic and non-syndromic polydactyly in two Indian families</title><source>Access via Wiley Online Library</source><creator>Patel, Rashmi ; Singh, Chandra Bhan ; Bhattacharya, Visweswar ; Singh, Subodh Kumar ; Ali, Akhtar</creator><creatorcontrib>Patel, Rashmi ; Singh, Chandra Bhan ; Bhattacharya, Visweswar ; Singh, Subodh Kumar ; Ali, Akhtar</creatorcontrib><identifier>ISSN: 0914-3505</identifier><identifier>EISSN: 1741-4520</identifier><identifier>DOI: 10.1111/cga.12139</identifier><language>eng</language><publisher>Blackwell Publishing Ltd</publisher><subject>Greig Cephalopolysyndactyly Syndrome ; India ; limb defects ; mutation ; polydactyly</subject><ispartof>Congenital Anomalies, 2016, Vol.56 (2), p.94-97</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784,4490,27925</link.rule.ids></links><search><creatorcontrib>Patel, Rashmi</creatorcontrib><creatorcontrib>Singh, Chandra Bhan</creatorcontrib><creatorcontrib>Bhattacharya, Visweswar</creatorcontrib><creatorcontrib>Singh, Subodh Kumar</creatorcontrib><creatorcontrib>Ali, Akhtar</creatorcontrib><title>GLI3 mutations in syndromic and non-syndromic polydactyly in two Indian families</title><title>Congenital Anomalies</title><addtitle>Congenital Anomalies</addtitle><subject>Greig Cephalopolysyndactyly Syndrome</subject><subject>India</subject><subject>limb defects</subject><subject>mutation</subject><subject>polydactyly</subject><issn>0914-3505</issn><issn>1741-4520</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2016</creationdate><recordtype>report</recordtype><recordid>eNqVis2KwjAYAIO4YHX34BvkBeImTdPQs2h1EREseAwf_VmibVKaiObtdwXBs3MZGAahOaML9s93-QsLFjOejVDEZMJIImI6RhHNWEK4oGKCps6dKY3TVNIIHfLdluPu6sFraxzWBrtgqsF2usRgKmysIa_S2zZUUPrQhsfqbxZvTaXB4AY63erafaKPBlpXfz09Q2S9KpYbop2v76ofdAdDUDBcVCq5FOq0z1URZ_L4w4Qq-Lv_H20BSrw</recordid><startdate>201603</startdate><enddate>201603</enddate><creator>Patel, Rashmi</creator><creator>Singh, Chandra Bhan</creator><creator>Bhattacharya, Visweswar</creator><creator>Singh, Subodh Kumar</creator><creator>Ali, Akhtar</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope></search><sort><creationdate>201603</creationdate><title>GLI3 mutations in syndromic and non-syndromic polydactyly in two Indian families</title><author>Patel, Rashmi ; Singh, Chandra Bhan ; Bhattacharya, Visweswar ; Singh, Subodh Kumar ; Ali, Akhtar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-istex_primary_ark_67375_WNG_T297SJ15_T3</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Greig Cephalopolysyndactyly Syndrome</topic><topic>India</topic><topic>limb defects</topic><topic>mutation</topic><topic>polydactyly</topic><toplevel>online_resources</toplevel><creatorcontrib>Patel, Rashmi</creatorcontrib><creatorcontrib>Singh, Chandra Bhan</creatorcontrib><creatorcontrib>Bhattacharya, Visweswar</creatorcontrib><creatorcontrib>Singh, Subodh Kumar</creatorcontrib><creatorcontrib>Ali, Akhtar</creatorcontrib><collection>Istex</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patel, Rashmi</au><au>Singh, Chandra Bhan</au><au>Bhattacharya, Visweswar</au><au>Singh, Subodh Kumar</au><au>Ali, Akhtar</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>GLI3 mutations in syndromic and non-syndromic polydactyly in two Indian families</atitle><jtitle>Congenital Anomalies</jtitle><addtitle>Congenital Anomalies</addtitle><date>2016-03</date><risdate>2016</risdate><volume>56</volume><issue>2</issue><spage>94</spage><epage>97</epage><pages>94-97</pages><issn>0914-3505</issn><eissn>1741-4520</eissn><pub>Blackwell Publishing Ltd</pub><doi>10.1111/cga.12139</doi></addata></record>
fulltext	fulltext
identifier	ISSN: 0914-3505
ispartof	Congenital Anomalies, 2016, Vol.56 (2), p.94-97
issn	0914-3505 1741-4520
language	eng
recordid	cdi_istex_primary_ark_67375_WNG_T297SJ15_T
source	Access via Wiley Online Library
subjects	Greig Cephalopolysyndactyly Syndrome India limb defects mutation polydactyly
title	GLI3 mutations in syndromic and non-syndromic polydactyly in two Indian families
url	https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T03%3A01%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.atitle=GLI3%20mutations%20in%20syndromic%20and%20non-syndromic%20polydactyly%20in%20two%20Indian%20families&rft.jtitle=Congenital%20Anomalies&rft.au=Patel,%20Rashmi&rft.date=2016-03&rft.volume=56&rft.issue=2&rft.spage=94&rft.epage=97&rft.pages=94-97&rft.issn=0914-3505&rft.eissn=1741-4520&rft_id=info:doi/10.1111/cga.12139&rft_dat=%3Cistex%3Eark_67375_WNG_T297SJ15_T%3C/istex%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true