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Delineation of dual molecular diagnosis in patients with skeletal deformity.

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Title: Delineation of dual molecular diagnosis in patients with skeletal deformity.
Authors: Liu, Lian1,2,3,4 (AUTHOR), Sun, Liying5 (AUTHOR), Chen, Yujun6 (AUTHOR), Wang, Muchuan1,2,3,4 (AUTHOR), Yu, Chenxi7 (AUTHOR), Huang, Yingzhao1,3,4 (AUTHOR), Zhao, Sen1,3,4 (AUTHOR), Du, Huakang1,3,4 (AUTHOR), Chen, Shaoke6 (AUTHOR), Fan, Xin6 (AUTHOR), Tian, Wen5 (AUTHOR), Wu, Zhihong3,4 (AUTHOR), Qiu, Guixing1,3,4 (AUTHOR) qiuguixingpumch@126.com, Zhang, Terry Jianguo1,3,4 (AUTHOR) pumczjg@sina.com, Wu, Nan1,3,4 (AUTHOR) dr.wunan@pumch.cn, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study group (CORPORATE AUTHOR)
Source: Orphanet Journal of Rare Diseases. 3/28/2022, Vol. 17 Issue 1, p1-9. 9p.
Database: Academic Search Ultimate
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An: 156274194
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PubType: Academic Journal
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  Data: Delineation of dual molecular diagnosis in patients with skeletal deformity.
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  Data: <searchLink fieldCode="AR" term="%22Liu%2C+Lian%22">Liu, Lian</searchLink><relatesTo>1,2,3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sun%2C+Liying%22">Sun, Liying</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chen%2C+Yujun%22">Chen, Yujun</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Muchuan%22">Wang, Muchuan</searchLink><relatesTo>1,2,3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yu%2C+Chenxi%22">Yu, Chenxi</searchLink><relatesTo>7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Huang%2C+Yingzhao%22">Huang, Yingzhao</searchLink><relatesTo>1,3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhao%2C+Sen%22">Zhao, Sen</searchLink><relatesTo>1,3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Du%2C+Huakang%22">Du, Huakang</searchLink><relatesTo>1,3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chen%2C+Shaoke%22">Chen, Shaoke</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fan%2C+Xin%22">Fan, Xin</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Tian%2C+Wen%22">Tian, Wen</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wu%2C+Zhihong%22">Wu, Zhihong</searchLink><relatesTo>3,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Qiu%2C+Guixing%22">Qiu, Guixing</searchLink><relatesTo>1,3,4</relatesTo> (AUTHOR)<i> qiuguixingpumch@126.com</i><br /><searchLink fieldCode="AR" term="%22Zhang%2C+Terry+Jianguo%22">Zhang, Terry Jianguo</searchLink><relatesTo>1,3,4</relatesTo> (AUTHOR)<i> pumczjg@sina.com</i><br /><searchLink fieldCode="AR" term="%22Wu%2C+Nan%22">Wu, Nan</searchLink><relatesTo>1,3,4</relatesTo> (AUTHOR)<i> dr.wunan@pumch.cn</i><br /><searchLink fieldCode="AR" term="%22Deciphering+Disorders+Involving+Scoliosis+and+COmorbidities+%28DISCO%29+study+group%22">Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study group</searchLink> (CORPORATE AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 3/28/2022, Vol. 17 Issue 1, p1-9. 9p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=156274194
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        Value: 10.1186/s13023-022-02293-x
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        Text: English
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              M: 03
              Text: 3/28/2022
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              Y: 2022
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