Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry.
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| Title: | Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry. |
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| Authors: | Brimble, Elise1 (AUTHOR) elli.brimble@invitae.com, Reyes, Kathryn G.2 (AUTHOR), Kuhathaas, Kopika3 (AUTHOR), Devinsky, Orrin4 (AUTHOR), Ruzhnikov, Maura R. Z.5 (AUTHOR), Ortiz-Gonzalez, Xilma R.6 (AUTHOR), Scheffer, Ingrid7 (AUTHOR), Bahi-Buisson, Nadia8 (AUTHOR), Olson, Heather9 (AUTHOR) |
| Source: | Orphanet Journal of Rare Diseases. 6/12/2023, Vol. 18 Issue 1, p1-10. 10p. |
| 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: 164264137 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Brimble%2C+Elise%22">Brimble, Elise</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> elli.brimble@invitae.com</i><br /><searchLink fieldCode="AR" term="%22Reyes%2C+Kathryn+G%2E%22">Reyes, Kathryn G.</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kuhathaas%2C+Kopika%22">Kuhathaas, Kopika</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Devinsky%2C+Orrin%22">Devinsky, Orrin</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ruzhnikov%2C+Maura+R%2E+Z%2E%22">Ruzhnikov, Maura R. Z.</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ortiz-Gonzalez%2C+Xilma+R%2E%22">Ortiz-Gonzalez, Xilma R.</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Scheffer%2C+Ingrid%22">Scheffer, Ingrid</searchLink><relatesTo>7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bahi-Buisson%2C+Nadia%22">Bahi-Buisson, Nadia</searchLink><relatesTo>8</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Olson%2C+Heather%22">Olson, Heather</searchLink><relatesTo>9</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 6/12/2023, Vol. 18 Issue 1, p1-10. 10p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=164264137 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-023-02745-y Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 10 StartPage: 1 Titles: – TitleFull: Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Brimble, Elise – PersonEntity: Name: NameFull: Reyes, Kathryn G. – PersonEntity: Name: NameFull: Kuhathaas, Kopika – PersonEntity: Name: NameFull: Devinsky, Orrin – PersonEntity: Name: NameFull: Ruzhnikov, Maura R. Z. – PersonEntity: Name: NameFull: Ortiz-Gonzalez, Xilma R. – PersonEntity: Name: NameFull: Scheffer, Ingrid – PersonEntity: Name: NameFull: Bahi-Buisson, Nadia – PersonEntity: Name: NameFull: Olson, Heather IsPartOfRelationships: – BibEntity: Dates: – D: 12 M: 06 Text: 6/12/2023 Type: published Y: 2023 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 18 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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