Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation.
Saved in:
| Title: | Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation. |
|---|---|
| Authors: | Frühmesser, Anne1, Blake, Jonathon2, Haberlandt, Edda3, Baying, Bianka2, Raeder, Benjamin4, Runz, Heiko5, Spreiz, Ana1, Fauth, Christine1, Benes, Vladimir2, Utermann, Gerd1, Zschocke, Johannes1, Kotzot, Dieter1 |
| Source: | European Journal of Human Genetics. Oct2013, Vol. 21 Issue 10, p1177-1180. 4p. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
|---|---|
| Header | DbId: asn DbLabel: Academic Search Ultimate An: 90285693 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Frühmesser%2C+Anne%22">Frühmesser, Anne</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Blake%2C+Jonathon%22">Blake, Jonathon</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Haberlandt%2C+Edda%22">Haberlandt, Edda</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Baying%2C+Bianka%22">Baying, Bianka</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Raeder%2C+Benjamin%22">Raeder, Benjamin</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Runz%2C+Heiko%22">Runz, Heiko</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Spreiz%2C+Ana%22">Spreiz, Ana</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Fauth%2C+Christine%22">Fauth, Christine</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Benes%2C+Vladimir%22">Benes, Vladimir</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Utermann%2C+Gerd%22">Utermann, Gerd</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Zschocke%2C+Johannes%22">Zschocke, Johannes</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Kotzot%2C+Dieter%22">Kotzot, Dieter</searchLink><relatesTo>1</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Human+Genetics%22">European Journal of Human Genetics</searchLink>. Oct2013, Vol. 21 Issue 10, p1177-1180. 4p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=90285693 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/ejhg.2013.18 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 4 StartPage: 1177 Titles: – TitleFull: Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Frühmesser, Anne – PersonEntity: Name: NameFull: Blake, Jonathon – PersonEntity: Name: NameFull: Haberlandt, Edda – PersonEntity: Name: NameFull: Baying, Bianka – PersonEntity: Name: NameFull: Raeder, Benjamin – PersonEntity: Name: NameFull: Runz, Heiko – PersonEntity: Name: NameFull: Spreiz, Ana – PersonEntity: Name: NameFull: Fauth, Christine – PersonEntity: Name: NameFull: Benes, Vladimir – PersonEntity: Name: NameFull: Utermann, Gerd – PersonEntity: Name: NameFull: Zschocke, Johannes – PersonEntity: Name: NameFull: Kotzot, Dieter IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: Oct2013 Type: published Y: 2013 Identifiers: – Type: issn-print Value: 10184813 Numbering: – Type: volume Value: 21 – Type: issue Value: 10 Titles: – TitleFull: European Journal of Human Genetics Type: main |
| ResultId | 1 |