Genetic and prenatal findings in two Japanese patients with Schinzel-Giedion syndrome

Saved in:
Bibliographic Details
Published in:Clinical case reports 2017, Vol.5 (1), p.5-8
Main Authors: Hishimura, Nozomi, Watari, Michiko, Ohata, Hiroki, Fuseya, Naho, Wakiguchi, Sadae, Tokutomi, Tomoharu, Okuhara, Kouji, Takahashi, Nobuhiro, Iizuka, Susumu, Yamamoto, Hiroshi, Mishima, Takashi, Fujieda, Satoko, Kobayashi, Ryoji, Cho, Kazutoshi, Kuroda, Yukiko, Kurosawa, Kenji, Tonoki, Hidefumi
Format: Report
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 8
container_issue 1
container_start_page 5
container_title Clinical case reports
container_volume 5
creator Hishimura, Nozomi
Watari, Michiko
Ohata, Hiroki
Fuseya, Naho
Wakiguchi, Sadae
Tokutomi, Tomoharu
Okuhara, Kouji
Takahashi, Nobuhiro
Iizuka, Susumu
Yamamoto, Hiroshi
Mishima, Takashi
Fujieda, Satoko
Kobayashi, Ryoji
Cho, Kazutoshi
Kuroda, Yukiko
Kurosawa, Kenji
Tonoki, Hidefumi
description
doi_str_mv 10.1002/ccr3.738
format report
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_1861564760</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1861564760</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_18615647603</originalsourceid><addsrcrecordid>eNqVjLtuwkAQAE8RkYIIUj5hSxrDno1tUiMeooXU6HRewkbHnuM9hODroUiRlmqmGI0xHxbHFjGfeN8V47qYvZh-jiVm-InT3j9_M0PVH0S0WOelxb75WpFQYg9OGmg7EpdcgANLw_KtwALpEmHjWiekBK1LTJIULpyOsPVHlhuFbMXUcBTQqzRdPNG7eT24oDT848CMlovdfJ21Xfw9k6b9idVTCI9rPOvezipbVtO6wuKJ9A63t0rD</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>report</recordtype><pqid>1861564760</pqid></control><display><type>report</type><title>Genetic and prenatal findings in two Japanese patients with Schinzel-Giedion syndrome</title><source>Publicly Available Content Database</source><source>PubMed</source><source>Wiley-Blackwell Open Access Titles(OpenAccess)</source><creator>Hishimura, Nozomi ; Watari, Michiko ; Ohata, Hiroki ; Fuseya, Naho ; Wakiguchi, Sadae ; Tokutomi, Tomoharu ; Okuhara, Kouji ; Takahashi, Nobuhiro ; Iizuka, Susumu ; Yamamoto, Hiroshi ; Mishima, Takashi ; Fujieda, Satoko ; Kobayashi, Ryoji ; Cho, Kazutoshi ; Kuroda, Yukiko ; Kurosawa, Kenji ; Tonoki, Hidefumi</creator><creatorcontrib>Hishimura, Nozomi ; Watari, Michiko ; Ohata, Hiroki ; Fuseya, Naho ; Wakiguchi, Sadae ; Tokutomi, Tomoharu ; Okuhara, Kouji ; Takahashi, Nobuhiro ; Iizuka, Susumu ; Yamamoto, Hiroshi ; Mishima, Takashi ; Fujieda, Satoko ; Kobayashi, Ryoji ; Cho, Kazutoshi ; Kuroda, Yukiko ; Kurosawa, Kenji ; Tonoki, Hidefumi</creatorcontrib><identifier>ISSN: 2050-0904</identifier><identifier>EISSN: 2050-0904</identifier><identifier>DOI: 10.1002/ccr3.738</identifier><language>eng</language><ispartof>Clinical case reports, 2017, Vol.5 (1), p.5-8</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784,4490,27925,37013</link.rule.ids></links><search><creatorcontrib>Hishimura, Nozomi</creatorcontrib><creatorcontrib>Watari, Michiko</creatorcontrib><creatorcontrib>Ohata, Hiroki</creatorcontrib><creatorcontrib>Fuseya, Naho</creatorcontrib><creatorcontrib>Wakiguchi, Sadae</creatorcontrib><creatorcontrib>Tokutomi, Tomoharu</creatorcontrib><creatorcontrib>Okuhara, Kouji</creatorcontrib><creatorcontrib>Takahashi, Nobuhiro</creatorcontrib><creatorcontrib>Iizuka, Susumu</creatorcontrib><creatorcontrib>Yamamoto, Hiroshi</creatorcontrib><creatorcontrib>Mishima, Takashi</creatorcontrib><creatorcontrib>Fujieda, Satoko</creatorcontrib><creatorcontrib>Kobayashi, Ryoji</creatorcontrib><creatorcontrib>Cho, Kazutoshi</creatorcontrib><creatorcontrib>Kuroda, Yukiko</creatorcontrib><creatorcontrib>Kurosawa, Kenji</creatorcontrib><creatorcontrib>Tonoki, Hidefumi</creatorcontrib><title>Genetic and prenatal findings in two Japanese patients with Schinzel-Giedion syndrome</title><title>Clinical case reports</title><issn>2050-0904</issn><issn>2050-0904</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2017</creationdate><recordtype>report</recordtype><recordid>eNqVjLtuwkAQAE8RkYIIUj5hSxrDno1tUiMeooXU6HRewkbHnuM9hODroUiRlmqmGI0xHxbHFjGfeN8V47qYvZh-jiVm-InT3j9_M0PVH0S0WOelxb75WpFQYg9OGmg7EpdcgANLw_KtwALpEmHjWiekBK1LTJIULpyOsPVHlhuFbMXUcBTQqzRdPNG7eT24oDT848CMlovdfJ21Xfw9k6b9idVTCI9rPOvezipbVtO6wuKJ9A63t0rD</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Hishimura, Nozomi</creator><creator>Watari, Michiko</creator><creator>Ohata, Hiroki</creator><creator>Fuseya, Naho</creator><creator>Wakiguchi, Sadae</creator><creator>Tokutomi, Tomoharu</creator><creator>Okuhara, Kouji</creator><creator>Takahashi, Nobuhiro</creator><creator>Iizuka, Susumu</creator><creator>Yamamoto, Hiroshi</creator><creator>Mishima, Takashi</creator><creator>Fujieda, Satoko</creator><creator>Kobayashi, Ryoji</creator><creator>Cho, Kazutoshi</creator><creator>Kuroda, Yukiko</creator><creator>Kurosawa, Kenji</creator><creator>Tonoki, Hidefumi</creator><scope>7X8</scope></search><sort><creationdate>20170101</creationdate><title>Genetic and prenatal findings in two Japanese patients with Schinzel-Giedion syndrome</title><author>Hishimura, Nozomi ; Watari, Michiko ; Ohata, Hiroki ; Fuseya, Naho ; Wakiguchi, Sadae ; Tokutomi, Tomoharu ; Okuhara, Kouji ; Takahashi, Nobuhiro ; Iizuka, Susumu ; Yamamoto, Hiroshi ; Mishima, Takashi ; Fujieda, Satoko ; Kobayashi, Ryoji ; Cho, Kazutoshi ; Kuroda, Yukiko ; Kurosawa, Kenji ; Tonoki, Hidefumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_18615647603</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Hishimura, Nozomi</creatorcontrib><creatorcontrib>Watari, Michiko</creatorcontrib><creatorcontrib>Ohata, Hiroki</creatorcontrib><creatorcontrib>Fuseya, Naho</creatorcontrib><creatorcontrib>Wakiguchi, Sadae</creatorcontrib><creatorcontrib>Tokutomi, Tomoharu</creatorcontrib><creatorcontrib>Okuhara, Kouji</creatorcontrib><creatorcontrib>Takahashi, Nobuhiro</creatorcontrib><creatorcontrib>Iizuka, Susumu</creatorcontrib><creatorcontrib>Yamamoto, Hiroshi</creatorcontrib><creatorcontrib>Mishima, Takashi</creatorcontrib><creatorcontrib>Fujieda, Satoko</creatorcontrib><creatorcontrib>Kobayashi, Ryoji</creatorcontrib><creatorcontrib>Cho, Kazutoshi</creatorcontrib><creatorcontrib>Kuroda, Yukiko</creatorcontrib><creatorcontrib>Kurosawa, Kenji</creatorcontrib><creatorcontrib>Tonoki, Hidefumi</creatorcontrib><collection>MEDLINE - Academic</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hishimura, Nozomi</au><au>Watari, Michiko</au><au>Ohata, Hiroki</au><au>Fuseya, Naho</au><au>Wakiguchi, Sadae</au><au>Tokutomi, Tomoharu</au><au>Okuhara, Kouji</au><au>Takahashi, Nobuhiro</au><au>Iizuka, Susumu</au><au>Yamamoto, Hiroshi</au><au>Mishima, Takashi</au><au>Fujieda, Satoko</au><au>Kobayashi, Ryoji</au><au>Cho, Kazutoshi</au><au>Kuroda, Yukiko</au><au>Kurosawa, Kenji</au><au>Tonoki, Hidefumi</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>Genetic and prenatal findings in two Japanese patients with Schinzel-Giedion syndrome</atitle><jtitle>Clinical case reports</jtitle><date>2017-01-01</date><risdate>2017</risdate><volume>5</volume><issue>1</issue><spage>5</spage><epage>8</epage><pages>5-8</pages><issn>2050-0904</issn><eissn>2050-0904</eissn><doi>10.1002/ccr3.738</doi></addata></record>
fulltext fulltext
identifier ISSN: 2050-0904
ispartof Clinical case reports, 2017, Vol.5 (1), p.5-8
issn 2050-0904
2050-0904
language eng
recordid cdi_proquest_miscellaneous_1861564760
source Publicly Available Content Database; PubMed; Wiley-Blackwell Open Access Titles(OpenAccess)
title Genetic and prenatal findings in two Japanese patients with Schinzel-Giedion syndrome
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T18%3A59%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.atitle=Genetic%20and%20prenatal%20findings%20in%20two%20Japanese%20patients%20with%20Schinzel-Giedion%20syndrome&rft.jtitle=Clinical%20case%20reports&rft.au=Hishimura,%20Nozomi&rft.date=2017-01-01&rft.volume=5&rft.issue=1&rft.spage=5&rft.epage=8&rft.pages=5-8&rft.issn=2050-0904&rft.eissn=2050-0904&rft_id=info:doi/10.1002/ccr3.738&rft_dat=%3Cproquest%3E1861564760%3C/proquest%3E%3Cgrp_id%3Ecdi_FETCH-proquest_miscellaneous_18615647603%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1861564760&rft_id=info:pmid/&rfr_iscdi=true