Different mutations in TBL1XR1 lead to diverse phenotypes of neurodevelopmental disorder: two case reports.
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| Title: | Different mutations in TBL1XR1 lead to diverse phenotypes of neurodevelopmental disorder: two case reports. |
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| Authors: | Wei, Linlin1 (AUTHOR), Yang, Yonghui2 (AUTHOR), Jiang, Tiejia1 (AUTHOR), Zhang, Chaolang1 (AUTHOR), Chen, Cuiying1 (AUTHOR), Huang, Mingwei3 (AUTHOR), Li, Nannan3 (AUTHOR) linannan@aegicare.cn, Xiong, Huachun2 (AUTHOR) xhczwy@sina.com, Gao, Feng1 (AUTHOR) chjjd@zju.edu.cn |
| Source: | BMC Medical Genomics. 7/17/2025, Vol. 18 Issue 1, p1-7. 7p. |
| 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: 186712131 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Different mutations in TBL1XR1 lead to diverse phenotypes of neurodevelopmental disorder: two case reports. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Wei%2C+Linlin%22">Wei, Linlin</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yang%2C+Yonghui%22">Yang, Yonghui</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jiang%2C+Tiejia%22">Jiang, Tiejia</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Chaolang%22">Zhang, Chaolang</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chen%2C+Cuiying%22">Chen, Cuiying</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Huang%2C+Mingwei%22">Huang, Mingwei</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Nannan%22">Li, Nannan</searchLink><relatesTo>3</relatesTo> (AUTHOR)<i> linannan@aegicare.cn</i><br /><searchLink fieldCode="AR" term="%22Xiong%2C+Huachun%22">Xiong, Huachun</searchLink><relatesTo>2</relatesTo> (AUTHOR)<i> xhczwy@sina.com</i><br /><searchLink fieldCode="AR" term="%22Gao%2C+Feng%22">Gao, Feng</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> chjjd@zju.edu.cn</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genomics%22">BMC Medical Genomics</searchLink>. 7/17/2025, Vol. 18 Issue 1, p1-7. 7p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=186712131 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s12920-025-02169-6 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 1 Titles: – TitleFull: Different mutations in TBL1XR1 lead to diverse phenotypes of neurodevelopmental disorder: two case reports. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Wei, Linlin – PersonEntity: Name: NameFull: Yang, Yonghui – PersonEntity: Name: NameFull: Jiang, Tiejia – PersonEntity: Name: NameFull: Zhang, Chaolang – PersonEntity: Name: NameFull: Chen, Cuiying – PersonEntity: Name: NameFull: Huang, Mingwei – PersonEntity: Name: NameFull: Li, Nannan – PersonEntity: Name: NameFull: Xiong, Huachun – PersonEntity: Name: NameFull: Gao, Feng IsPartOfRelationships: – BibEntity: Dates: – D: 17 M: 07 Text: 7/17/2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 17558794 Numbering: – Type: volume Value: 18 – Type: issue Value: 1 Titles: – TitleFull: BMC Medical Genomics Type: main |
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