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Whole exome sequencing enhances diagnosis of hereditary bronchiectasis.

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Title: Whole exome sequencing enhances diagnosis of hereditary bronchiectasis.
Authors: Zhou, Wangji1,2 (AUTHOR), Li, Yixuan3 (AUTHOR), Zheng, Haixia4 (AUTHOR), He, Miao4 (AUTHOR), Zhang, Miaoyan1 (AUTHOR), Chen, Qiaoling1 (AUTHOR), Situ, Christopher5 (AUTHOR), Wang, Yaqi1 (AUTHOR), Zhang, Ting1 (AUTHOR), Chen, Keqi1 (AUTHOR), Dai, Jinrong1 (AUTHOR), Meng, Shuzhen1 (AUTHOR), Liu, Xueqi1 (AUTHOR), Wu, Aohua1 (AUTHOR), Liu, Yaping3 (AUTHOR) ypliu_pumc@163.com, Xu, Kai-Feng1 (AUTHOR), Tian, Xinlun1,2 (AUTHOR) xinlun_t@sina.com, Zhang, Xue4 (AUTHOR)
Source: Orphanet Journal of Rare Diseases. 3/24/2025, Vol. 20 Issue 1, p1-8. 8p.
Database: Academic Search Ultimate
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Header DbId: asn
DbLabel: Academic Search Ultimate
An: 183972315
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PubType: Academic Journal
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  Data: Whole exome sequencing enhances diagnosis of hereditary bronchiectasis.
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  Data: <searchLink fieldCode="AR" term="%22Zhou%2C+Wangji%22">Zhou, Wangji</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Yixuan%22">Li, Yixuan</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zheng%2C+Haixia%22">Zheng, Haixia</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22He%2C+Miao%22">He, Miao</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Miaoyan%22">Zhang, Miaoyan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chen%2C+Qiaoling%22">Chen, Qiaoling</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Situ%2C+Christopher%22">Situ, Christopher</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Yaqi%22">Wang, Yaqi</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Ting%22">Zhang, Ting</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chen%2C+Keqi%22">Chen, Keqi</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Dai%2C+Jinrong%22">Dai, Jinrong</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Meng%2C+Shuzhen%22">Meng, Shuzhen</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Liu%2C+Xueqi%22">Liu, Xueqi</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wu%2C+Aohua%22">Wu, Aohua</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Liu%2C+Yaping%22">Liu, Yaping</searchLink><relatesTo>3</relatesTo> (AUTHOR)<i> ypliu_pumc@163.com</i><br /><searchLink fieldCode="AR" term="%22Xu%2C+Kai-Feng%22">Xu, Kai-Feng</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Tian%2C+Xinlun%22">Tian, Xinlun</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> xinlun_t@sina.com</i><br /><searchLink fieldCode="AR" term="%22Zhang%2C+Xue%22">Zhang, Xue</searchLink><relatesTo>4</relatesTo> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 3/24/2025, Vol. 20 Issue 1, p1-8. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=183972315
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        Value: 10.1186/s13023-025-03661-z
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        Text: English
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      – TitleFull: Whole exome sequencing enhances diagnosis of hereditary bronchiectasis.
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              M: 03
              Text: 3/24/2025
              Type: published
              Y: 2025
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