Clinical features and novel pathogenic variants of patients with Behçet's disease like trisomy 8.
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| Title: | Clinical features and novel pathogenic variants of patients with Behçet's disease like trisomy 8. |
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| Authors: | Ding, Xingru1 (AUTHOR), Yang, Jinghan2 (AUTHOR), Han, Xiao1 (AUTHOR), Shen, Yi-Fan3 (AUTHOR), Yang, Kangkang1 (AUTHOR), Shangguan, Yaoyao1 (AUTHOR), Dong, Yiwei1 (AUTHOR), Ye, Xiaohua1 (AUTHOR) yxh205020@163.com |
| Source: | Orphanet Journal of Rare Diseases. 7/4/2025, Vol. 20 Issue 1, p1-11. 11p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 186463427 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Clinical features and novel pathogenic variants of patients with Behçet's disease like trisomy 8. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Ding%2C+Xingru%22">Ding, Xingru</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yang%2C+Jinghan%22">Yang, Jinghan</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Han%2C+Xiao%22">Han, Xiao</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Shen%2C+Yi-Fan%22">Shen, Yi-Fan</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yang%2C+Kangkang%22">Yang, Kangkang</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Shangguan%2C+Yaoyao%22">Shangguan, Yaoyao</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Dong%2C+Yiwei%22">Dong, Yiwei</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ye%2C+Xiaohua%22">Ye, Xiaohua</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> yxh205020@163.com</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 7/4/2025, Vol. 20 Issue 1, p1-11. 11p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=186463427 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-025-03878-y Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 1 Titles: – TitleFull: Clinical features and novel pathogenic variants of patients with Behçet's disease like trisomy 8. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ding, Xingru – PersonEntity: Name: NameFull: Yang, Jinghan – PersonEntity: Name: NameFull: Han, Xiao – PersonEntity: Name: NameFull: Shen, Yi-Fan – PersonEntity: Name: NameFull: Yang, Kangkang – PersonEntity: Name: NameFull: Shangguan, Yaoyao – PersonEntity: Name: NameFull: Dong, Yiwei – PersonEntity: Name: NameFull: Ye, Xiaohua IsPartOfRelationships: – BibEntity: Dates: – D: 04 M: 07 Text: 7/4/2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 20 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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