A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4.
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| Title: | A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4. |
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| Authors: | Yang, Kun1 (AUTHOR), Wang, Xi2 (AUTHOR), Wang, Wei‐Qian2,3,4,5 (AUTHOR), Han, Ming‐Yu3,4,5 (AUTHOR), Hu, Li‐Min2 (AUTHOR), Kang, Dong‐Yang3,4,5 (AUTHOR), Yang, Jin‐Yuan3,4,5 (AUTHOR), Liu, Min2 (AUTHOR), Gao, Xue2 (AUTHOR) mixueer0110@126.com, Yuan, Yong‐Yi3,4,5 (AUTHOR) yyymzh@163.com, Xu, Jin‐Cao2 (AUTHOR) xujincao@126.com |
| Source: | Molecular Genetics & Genomic Medicine. Mar2023, Vol. 11 Issue 3, p1-15. 15p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 162381105 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=162381105 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/mgg3.2103 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 15 StartPage: 1 Titles: – TitleFull: A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Yang, Kun – PersonEntity: Name: NameFull: Wang, Xi – PersonEntity: Name: NameFull: Wang, Wei‐Qian – PersonEntity: Name: NameFull: Han, Ming‐Yu – PersonEntity: Name: NameFull: Hu, Li‐Min – PersonEntity: Name: NameFull: Kang, Dong‐Yang – PersonEntity: Name: NameFull: Yang, Jin‐Yuan – PersonEntity: Name: NameFull: Liu, Min – PersonEntity: Name: NameFull: Gao, Xue – PersonEntity: Name: NameFull: Yuan, Yong‐Yi – PersonEntity: Name: NameFull: Xu, Jin‐Cao IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: Mar2023 Type: published Y: 2023 Identifiers: – Type: issn-print Value: 23249269 Numbering: – Type: volume Value: 11 – Type: issue Value: 3 Titles: – TitleFull: Molecular Genetics & Genomic Medicine Type: main |
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