Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith–Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted region.
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| Title: | Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith–Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted region. |
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| Authors: | Urakawa, Tatsuki1,2 (AUTHOR) urakawa-t@ncchd.go.jp, Kanamaru, Yuri1,3 (AUTHOR) kanamary@kuhp.kyoto-u.ac.jp, Amano, Naoko4 (AUTHOR) naokoam@keio.jp, Uchida, Akira5 (AUTHOR) qq6b4sp9k@yahoo.co.jp, Fukami, Maki1,6 (AUTHOR) fukami-m@ncchd.go.jp, Kagami, Masayo1 (AUTHOR) kagami-ms@ncchd.go.jp |
| Source: | Clinical Epigenetics. 6/9/2025, Vol. 17 Issue 1, p1-13. 13p. |
| 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: 185809951 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith–Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted region. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Urakawa%2C+Tatsuki%22">Urakawa, Tatsuki</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> urakawa-t@ncchd.go.jp</i><br /><searchLink fieldCode="AR" term="%22Kanamaru%2C+Yuri%22">Kanamaru, Yuri</searchLink><relatesTo>1,3</relatesTo> (AUTHOR)<i> kanamary@kuhp.kyoto-u.ac.jp</i><br /><searchLink fieldCode="AR" term="%22Amano%2C+Naoko%22">Amano, Naoko</searchLink><relatesTo>4</relatesTo> (AUTHOR)<i> naokoam@keio.jp</i><br /><searchLink fieldCode="AR" term="%22Uchida%2C+Akira%22">Uchida, Akira</searchLink><relatesTo>5</relatesTo> (AUTHOR)<i> qq6b4sp9k@yahoo.co.jp</i><br /><searchLink fieldCode="AR" term="%22Fukami%2C+Maki%22">Fukami, Maki</searchLink><relatesTo>1,6</relatesTo> (AUTHOR)<i> fukami-m@ncchd.go.jp</i><br /><searchLink fieldCode="AR" term="%22Kagami%2C+Masayo%22">Kagami, Masayo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> kagami-ms@ncchd.go.jp</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Clinical+Epigenetics%22">Clinical Epigenetics</searchLink>. 6/9/2025, Vol. 17 Issue 1, p1-13. 13p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=185809951 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13148-025-01907-y Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 13 StartPage: 1 Titles: – TitleFull: Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith–Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted region. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Urakawa, Tatsuki – PersonEntity: Name: NameFull: Kanamaru, Yuri – PersonEntity: Name: NameFull: Amano, Naoko – PersonEntity: Name: NameFull: Uchida, Akira – PersonEntity: Name: NameFull: Fukami, Maki – PersonEntity: Name: NameFull: Kagami, Masayo IsPartOfRelationships: – BibEntity: Dates: – D: 09 M: 06 Text: 6/9/2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 18687075 Numbering: – Type: volume Value: 17 – Type: issue Value: 1 Titles: – TitleFull: Clinical Epigenetics Type: main |
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