Face processing and exploration of social signals in Prader-Willi syndrome: a genetic signature.
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| Title: | Face processing and exploration of social signals in Prader-Willi syndrome: a genetic signature. |
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| Authors: | Debladis, Jimmy1,2,3 (AUTHOR) jimmy.debladis@cnrs.fr, Valette, Marion4 (AUTHOR), Strenilkov, Kuzma5 (AUTHOR), Mantoulan, Carine4 (AUTHOR), Thuilleaux, Denise6 (AUTHOR), Laurier, Virginie6 (AUTHOR), Molinas, Catherine4 (AUTHOR), Barone, Pascal1,2 (AUTHOR), Tauber, Maïthé4,7 (AUTHOR) |
| Source: | Orphanet Journal of Rare Diseases. 11/15/2019, Vol. 14 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: 139691634 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Face processing and exploration of social signals in Prader-Willi syndrome: a genetic signature. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Debladis%2C+Jimmy%22">Debladis, Jimmy</searchLink><relatesTo>1,2,3</relatesTo> (AUTHOR)<i> jimmy.debladis@cnrs.fr</i><br /><searchLink fieldCode="AR" term="%22Valette%2C+Marion%22">Valette, Marion</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Strenilkov%2C+Kuzma%22">Strenilkov, Kuzma</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mantoulan%2C+Carine%22">Mantoulan, Carine</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Thuilleaux%2C+Denise%22">Thuilleaux, Denise</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Laurier%2C+Virginie%22">Laurier, Virginie</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Molinas%2C+Catherine%22">Molinas, Catherine</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Barone%2C+Pascal%22">Barone, Pascal</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Tauber%2C+Maïthé%22">Tauber, Maïthé</searchLink><relatesTo>4,7</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>. 11/15/2019, Vol. 14 Issue 1, p1-13. 13p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=139691634 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-019-1221-3 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 13 StartPage: 1 Titles: – TitleFull: Face processing and exploration of social signals in Prader-Willi syndrome: a genetic signature. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Debladis, Jimmy – PersonEntity: Name: NameFull: Valette, Marion – PersonEntity: Name: NameFull: Strenilkov, Kuzma – PersonEntity: Name: NameFull: Mantoulan, Carine – PersonEntity: Name: NameFull: Thuilleaux, Denise – PersonEntity: Name: NameFull: Laurier, Virginie – PersonEntity: Name: NameFull: Molinas, Catherine – PersonEntity: Name: NameFull: Barone, Pascal – PersonEntity: Name: NameFull: Tauber, Maïthé IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 11 Text: 11/15/2019 Type: published Y: 2019 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 14 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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