MOESM1 of Broadening the phenotype of the TWNK gene associated Perrault syndrome
Additional file 1: Table S1. List of the genes used in the NGS panel.
Gespeichert in:
Hauptverfasser: | , , , , , , , , , |
---|---|
Format: | Bild |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | |
container_volume | |
creator | Fekete, Bálint Pentelényi, Klára Gabor Rudas Gál, Anikó Grosz, Zoltán Illés, Anett Jimoh Idris Gabor Csukly Domonkos, Andor Molnar, Maria |
description | Additional file 1: Table S1. List of the genes used in the NGS panel. |
doi_str_mv | 10.6084/m9.figshare.11406318 |
format | Image |
fullrecord | <record><control><sourceid>datacite_PQ8</sourceid><recordid>TN_cdi_datacite_primary_10_6084_m9_figshare_11406318</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_6084_m9_figshare_11406318</sourcerecordid><originalsourceid>FETCH-datacite_primary_10_6084_m9_figshare_114063183</originalsourceid><addsrcrecordid>eNqdzkEKwjAUBNBsXIh6Axf_AtaGltJulYog1YKCy_BpfttAk5QkLnp7KdgLuBqYYeAxtudxlMV5etRF1KrO9-go4jyNs4Tna1ZXj_JZcbAtnJxFSUaZDkJPMPZkbJhGmre5eL3vN-jIEKD3tlEYSEJNzuFnCOAnI53VtGWrFgdPu19uWHopX-frQWLARgUSo1Ma3SR4LGaY0IVYYGKBJX_evuwlS3g</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>image</recordtype></control><display><type>image</type><title>MOESM1 of Broadening the phenotype of the TWNK gene associated Perrault syndrome</title><source>DataCite</source><creator>Fekete, Bálint ; Pentelényi, Klára ; Gabor Rudas ; Gál, Anikó ; Grosz, Zoltán ; Illés, Anett ; Jimoh Idris ; Gabor Csukly ; Domonkos, Andor ; Molnar, Maria</creator><creatorcontrib>Fekete, Bálint ; Pentelényi, Klára ; Gabor Rudas ; Gál, Anikó ; Grosz, Zoltán ; Illés, Anett ; Jimoh Idris ; Gabor Csukly ; Domonkos, Andor ; Molnar, Maria</creatorcontrib><description>Additional file 1: Table S1. List of the genes used in the NGS panel.</description><identifier>DOI: 10.6084/m9.figshare.11406318</identifier><language>eng</language><publisher>figshare</publisher><subject>Biological Sciences not elsewhere classified ; Cancer ; Computational Biology ; Developmental Biology ; FOS: Biological sciences ; FOS: Health sciences ; Genetics ; Infectious Diseases ; Medicine ; Molecular Biology</subject><creationdate>2019</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,1894</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.11406318$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Fekete, Bálint</creatorcontrib><creatorcontrib>Pentelényi, Klára</creatorcontrib><creatorcontrib>Gabor Rudas</creatorcontrib><creatorcontrib>Gál, Anikó</creatorcontrib><creatorcontrib>Grosz, Zoltán</creatorcontrib><creatorcontrib>Illés, Anett</creatorcontrib><creatorcontrib>Jimoh Idris</creatorcontrib><creatorcontrib>Gabor Csukly</creatorcontrib><creatorcontrib>Domonkos, Andor</creatorcontrib><creatorcontrib>Molnar, Maria</creatorcontrib><title>MOESM1 of Broadening the phenotype of the TWNK gene associated Perrault syndrome</title><description>Additional file 1: Table S1. List of the genes used in the NGS panel.</description><subject>Biological Sciences not elsewhere classified</subject><subject>Cancer</subject><subject>Computational Biology</subject><subject>Developmental Biology</subject><subject>FOS: Biological sciences</subject><subject>FOS: Health sciences</subject><subject>Genetics</subject><subject>Infectious Diseases</subject><subject>Medicine</subject><subject>Molecular Biology</subject><fulltext>true</fulltext><rsrctype>image</rsrctype><creationdate>2019</creationdate><recordtype>image</recordtype><sourceid>PQ8</sourceid><recordid>eNqdzkEKwjAUBNBsXIh6Axf_AtaGltJulYog1YKCy_BpfttAk5QkLnp7KdgLuBqYYeAxtudxlMV5etRF1KrO9-go4jyNs4Tna1ZXj_JZcbAtnJxFSUaZDkJPMPZkbJhGmre5eL3vN-jIEKD3tlEYSEJNzuFnCOAnI53VtGWrFgdPu19uWHopX-frQWLARgUSo1Ma3SR4LGaY0IVYYGKBJX_evuwlS3g</recordid><startdate>20191219</startdate><enddate>20191219</enddate><creator>Fekete, Bálint</creator><creator>Pentelényi, Klára</creator><creator>Gabor Rudas</creator><creator>Gál, Anikó</creator><creator>Grosz, Zoltán</creator><creator>Illés, Anett</creator><creator>Jimoh Idris</creator><creator>Gabor Csukly</creator><creator>Domonkos, Andor</creator><creator>Molnar, Maria</creator><general>figshare</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20191219</creationdate><title>MOESM1 of Broadening the phenotype of the TWNK gene associated Perrault syndrome</title><author>Fekete, Bálint ; Pentelényi, Klára ; Gabor Rudas ; Gál, Anikó ; Grosz, Zoltán ; Illés, Anett ; Jimoh Idris ; Gabor Csukly ; Domonkos, Andor ; Molnar, Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_6084_m9_figshare_114063183</frbrgroupid><rsrctype>images</rsrctype><prefilter>images</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Biological Sciences not elsewhere classified</topic><topic>Cancer</topic><topic>Computational Biology</topic><topic>Developmental Biology</topic><topic>FOS: Biological sciences</topic><topic>FOS: Health sciences</topic><topic>Genetics</topic><topic>Infectious Diseases</topic><topic>Medicine</topic><topic>Molecular Biology</topic><toplevel>online_resources</toplevel><creatorcontrib>Fekete, Bálint</creatorcontrib><creatorcontrib>Pentelényi, Klára</creatorcontrib><creatorcontrib>Gabor Rudas</creatorcontrib><creatorcontrib>Gál, Anikó</creatorcontrib><creatorcontrib>Grosz, Zoltán</creatorcontrib><creatorcontrib>Illés, Anett</creatorcontrib><creatorcontrib>Jimoh Idris</creatorcontrib><creatorcontrib>Gabor Csukly</creatorcontrib><creatorcontrib>Domonkos, Andor</creatorcontrib><creatorcontrib>Molnar, Maria</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Fekete, Bálint</au><au>Pentelényi, Klára</au><au>Gabor Rudas</au><au>Gál, Anikó</au><au>Grosz, Zoltán</au><au>Illés, Anett</au><au>Jimoh Idris</au><au>Gabor Csukly</au><au>Domonkos, Andor</au><au>Molnar, Maria</au><format>book</format><genre>unknown</genre><ristype>GEN</ristype><title>MOESM1 of Broadening the phenotype of the TWNK gene associated Perrault syndrome</title><date>2019-12-19</date><risdate>2019</risdate><abstract>Additional file 1: Table S1. List of the genes used in the NGS panel.</abstract><pub>figshare</pub><doi>10.6084/m9.figshare.11406318</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | DOI: 10.6084/m9.figshare.11406318 |
ispartof | |
issn | |
language | eng |
recordid | cdi_datacite_primary_10_6084_m9_figshare_11406318 |
source | DataCite |
subjects | Biological Sciences not elsewhere classified Cancer Computational Biology Developmental Biology FOS: Biological sciences FOS: Health sciences Genetics Infectious Diseases Medicine Molecular Biology |
title | MOESM1 of Broadening the phenotype of the TWNK gene associated Perrault syndrome |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T13%3A05%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-datacite_PQ8&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.au=Fekete,%20B%C3%A1lint&rft.date=2019-12-19&rft_id=info:doi/10.6084/m9.figshare.11406318&rft_dat=%3Cdatacite_PQ8%3E10_6084_m9_figshare_11406318%3C/datacite_PQ8%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 |