High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey.
Saved in:
| Title: | High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey. |
|---|---|
| Authors: | Kalb, S1, Caglayan, AO2, Degerliyurt, A3, Schmid, S1, Ceylaner, S4, Hatipoglu, N5, Hinderhofer, K6, Rehder, H7, Kurtoglu, S8, Ceylaner, G4, Zschocke, J1, Witsch-Baumgartner, M1 |
| Source: | Clinical Genetics. Jun2012, Vol. 81 Issue 6, p598-601. 4p. 1 Color Photograph, 1 Chart. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
|---|---|
| Header | DbId: asn DbLabel: Academic Search Ultimate An: 74750832 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Kalb%2C+S%22">Kalb, S</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Caglayan%2C+AO%22">Caglayan, AO</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Degerliyurt%2C+A%22">Degerliyurt, A</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Schmid%2C+S%22">Schmid, S</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Ceylaner%2C+S%22">Ceylaner, S</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Hatipoglu%2C+N%22">Hatipoglu, N</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Hinderhofer%2C+K%22">Hinderhofer, K</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Rehder%2C+H%22">Rehder, H</searchLink><relatesTo>7</relatesTo><br /><searchLink fieldCode="AR" term="%22Kurtoglu%2C+S%22">Kurtoglu, S</searchLink><relatesTo>8</relatesTo><br /><searchLink fieldCode="AR" term="%22Ceylaner%2C+G%22">Ceylaner, G</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Zschocke%2C+J%22">Zschocke, J</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Witsch-Baumgartner%2C+M%22">Witsch-Baumgartner, M</searchLink><relatesTo>1</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Clinical+Genetics%22">Clinical Genetics</searchLink>. Jun2012, Vol. 81 Issue 6, p598-601. 4p. 1 Color Photograph, 1 Chart. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=74750832 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/j.1399-0004.2011.01750.x Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 4 StartPage: 598 Titles: – TitleFull: High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Kalb, S – PersonEntity: Name: NameFull: Caglayan, AO – PersonEntity: Name: NameFull: Degerliyurt, A – PersonEntity: Name: NameFull: Schmid, S – PersonEntity: Name: NameFull: Ceylaner, S – PersonEntity: Name: NameFull: Hatipoglu, N – PersonEntity: Name: NameFull: Hinderhofer, K – PersonEntity: Name: NameFull: Rehder, H – PersonEntity: Name: NameFull: Kurtoglu, S – PersonEntity: Name: NameFull: Ceylaner, G – PersonEntity: Name: NameFull: Zschocke, J – PersonEntity: Name: NameFull: Witsch-Baumgartner, M IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: Jun2012 Type: published Y: 2012 Identifiers: – Type: issn-print Value: 00099163 Numbering: – Type: volume Value: 81 – Type: issue Value: 6 Titles: – TitleFull: Clinical Genetics Type: main |
| ResultId | 1 |
