Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.
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| Title: | Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome. |
|---|---|
| Authors: | Wieland, I.1, Weidner, C.1, Ciccone, R.2, Lapi, E.3, McDonald-McGinn, D.4, Kress, W.5, Jakubiczka, S.1, Collmann, H.6, Zuffardi, O.2,7, Zackai, E.4, Wieacker, P.1,8 wieacker@uni-muenster.de |
| Source: | Clinical Genetics. Dec2007, Vol. 72 Issue 6, p506-516. 11p. 2 Diagrams, 5 Charts, 1 Graph. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 27448365 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Wieland%2C+I%2E%22">Wieland, I.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Weidner%2C+C%2E%22">Weidner, C.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Ciccone%2C+R%2E%22">Ciccone, R.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Lapi%2C+E%2E%22">Lapi, E.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22McDonald-McGinn%2C+D%2E%22">McDonald-McGinn, D.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Kress%2C+W%2E%22">Kress, W.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Jakubiczka%2C+S%2E%22">Jakubiczka, S.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Collmann%2C+H%2E%22">Collmann, H.</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Zuffardi%2C+O%2E%22">Zuffardi, O.</searchLink><relatesTo>2,7</relatesTo><br /><searchLink fieldCode="AR" term="%22Zackai%2C+E%2E%22">Zackai, E.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Wieacker%2C+P%2E%22">Wieacker, P.</searchLink><relatesTo>1,8</relatesTo><i> wieacker@uni-muenster.de</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Clinical+Genetics%22">Clinical Genetics</searchLink>. Dec2007, Vol. 72 Issue 6, p506-516. 11p. 2 Diagrams, 5 Charts, 1 Graph. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=27448365 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/j.1399-0004.2007.00905.x Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 506 Titles: – TitleFull: Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Wieland, I. – PersonEntity: Name: NameFull: Weidner, C. – PersonEntity: Name: NameFull: Ciccone, R. – PersonEntity: Name: NameFull: Lapi, E. – PersonEntity: Name: NameFull: McDonald-McGinn, D. – PersonEntity: Name: NameFull: Kress, W. – PersonEntity: Name: NameFull: Jakubiczka, S. – PersonEntity: Name: NameFull: Collmann, H. – PersonEntity: Name: NameFull: Zuffardi, O. – PersonEntity: Name: NameFull: Zackai, E. – PersonEntity: Name: NameFull: Wieacker, P. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: Dec2007 Type: published Y: 2007 Identifiers: – Type: issn-print Value: 00099163 Numbering: – Type: volume Value: 72 – Type: issue Value: 6 Titles: – TitleFull: Clinical Genetics Type: main |
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