Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4.
Saved in:
| Title: | Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4. |
|---|---|
| Authors: | Villavicencio-Lorini, Pablo1, Klopocki, Eva2, Trimborn, Marc3, Koll, Randi3, Mundlos, Stefan2, Horn, Denise3 |
| Source: | European Journal of Human Genetics. Jul2013, Vol. 21 Issue 7, p743-748. 6p. 1 Black and White Photograph, 1 Diagram, 1 Chart, 1 Graph. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
|---|---|
| Header | DbId: asn DbLabel: Academic Search Ultimate An: 88116977 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Villavicencio-Lorini%2C+Pablo%22">Villavicencio-Lorini, Pablo</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Klopocki%2C+Eva%22">Klopocki, Eva</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Trimborn%2C+Marc%22">Trimborn, Marc</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Koll%2C+Randi%22">Koll, Randi</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Mundlos%2C+Stefan%22">Mundlos, Stefan</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Horn%2C+Denise%22">Horn, Denise</searchLink><relatesTo>3</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Human+Genetics%22">European Journal of Human Genetics</searchLink>. Jul2013, Vol. 21 Issue 7, p743-748. 6p. 1 Black and White Photograph, 1 Diagram, 1 Chart, 1 Graph. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=88116977 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/ejhg.2012.240 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 6 StartPage: 743 Titles: – TitleFull: Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Villavicencio-Lorini, Pablo – PersonEntity: Name: NameFull: Klopocki, Eva – PersonEntity: Name: NameFull: Trimborn, Marc – PersonEntity: Name: NameFull: Koll, Randi – PersonEntity: Name: NameFull: Mundlos, Stefan – PersonEntity: Name: NameFull: Horn, Denise IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: Jul2013 Type: published Y: 2013 Identifiers: – Type: issn-print Value: 10184813 Numbering: – Type: volume Value: 21 – Type: issue Value: 7 Titles: – TitleFull: European Journal of Human Genetics Type: main |
| ResultId | 1 |