Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patients.
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| Title: | Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patients. |
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| Authors: | Zhao, Jianbo1 (AUTHOR) jianbo04429@126.com, Lyu, Guizhen2 (AUTHOR), Ding, Changhong1 (AUTHOR), Wang, Xiaohui1 (AUTHOR), Li, Jiuwei1 (AUTHOR), Zhang, Weihua1 (AUTHOR), Yang, Xinying1 (AUTHOR), Zhang, Victor Wei2 (AUTHOR) |
| Source: | Molecular Genetics & Genomic Medicine. Mar2022, Vol. 10 Issue 3, p1-16. 16p. |
| 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: 155782610 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patients. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Zhao%2C+Jianbo%22">Zhao, Jianbo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> jianbo04429@126.com</i><br /><searchLink fieldCode="AR" term="%22Lyu%2C+Guizhen%22">Lyu, Guizhen</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ding%2C+Changhong%22">Ding, Changhong</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Xiaohui%22">Wang, Xiaohui</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Jiuwei%22">Li, Jiuwei</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Weihua%22">Zhang, Weihua</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yang%2C+Xinying%22">Yang, Xinying</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Victor+Wei%22">Zhang, Victor Wei</searchLink><relatesTo>2</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Molecular+Genetics+%26+Genomic+Medicine%22">Molecular Genetics & Genomic Medicine</searchLink>. Mar2022, Vol. 10 Issue 3, p1-16. 16p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=155782610 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/mgg3.1825 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 16 StartPage: 1 Titles: – TitleFull: Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patients. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Zhao, Jianbo – PersonEntity: Name: NameFull: Lyu, Guizhen – PersonEntity: Name: NameFull: Ding, Changhong – PersonEntity: Name: NameFull: Wang, Xiaohui – PersonEntity: Name: NameFull: Li, Jiuwei – PersonEntity: Name: NameFull: Zhang, Weihua – PersonEntity: Name: NameFull: Yang, Xinying – PersonEntity: Name: NameFull: Zhang, Victor Wei IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: Mar2022 Type: published Y: 2022 Identifiers: – Type: issn-print Value: 23249269 Numbering: – Type: volume Value: 10 – Type: issue Value: 3 Titles: – TitleFull: Molecular Genetics & Genomic Medicine Type: main |
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