Neurodevelopmental disorder: Hao–Fountain syndrome with USP7 mutation—a case report.
Saved in:
| Title: | Neurodevelopmental disorder: Hao–Fountain syndrome with USP7 mutation—a case report. |
|---|---|
| Authors: | Rafeienejad, Fatemeh1 (AUTHOR), Keyhani, Elahe2 (AUTHOR), Akbarfahimi, Nazila1 (AUTHOR) nazilafahimi@gmail.com, Nouri, Narges3 (AUTHOR) |
| Source: | Journal of Medical Case Reports. 7/24/2025, Vol. 19 Issue 1, p1-5. 5p. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| FullText | Links: – Type: pdflink Text: Availability: 1 |
|---|---|
| Header | DbId: asn DbLabel: Academic Search Ultimate An: 186988201 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Neurodevelopmental disorder: Hao–Fountain syndrome with USP7 mutation—a case report. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Rafeienejad%2C+Fatemeh%22">Rafeienejad, Fatemeh</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Keyhani%2C+Elahe%22">Keyhani, Elahe</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Akbarfahimi%2C+Nazila%22">Akbarfahimi, Nazila</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> nazilafahimi@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Nouri%2C+Narges%22">Nouri, Narges</searchLink><relatesTo>3</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Journal+of+Medical+Case+Reports%22">Journal of Medical Case Reports</searchLink>. 7/24/2025, Vol. 19 Issue 1, p1-5. 5p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=186988201 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13256-025-05403-y Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 1 Titles: – TitleFull: Neurodevelopmental disorder: Hao–Fountain syndrome with USP7 mutation—a case report. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Rafeienejad, Fatemeh – PersonEntity: Name: NameFull: Keyhani, Elahe – PersonEntity: Name: NameFull: Akbarfahimi, Nazila – PersonEntity: Name: NameFull: Nouri, Narges IsPartOfRelationships: – BibEntity: Dates: – D: 24 M: 07 Text: 7/24/2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 17521947 Numbering: – Type: volume Value: 19 – Type: issue Value: 1 Titles: – TitleFull: Journal of Medical Case Reports Type: main |
| ResultId | 1 |