Drayer’s syndrome of mental retardation, microcephaly, short stature and absent phalanges is caused by a recurrent deletion of chromosome 15(q26.2→qter).
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| Title: | Drayer’s syndrome of mental retardation, microcephaly, short stature and absent phalanges is caused by a recurrent deletion of chromosome 15(q26.2→qter). |
|---|---|
| Authors: | Rump, P.1 p.rump@medgen.umcg.nl, Dijkhuizen, T.1, Sikkema-Raddatz, B.1, Lemmink, H. H.1, Vos, Y. J.1, Verheij, J. B. G. M.1, Van Ravenswaaij, C. M. A.1 |
| Source: | Clinical Genetics. Nov2008, Vol. 74 Issue 5, p455-462. 8p. 3 Black and White Photographs, 1 Diagram, 1 Chart, 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: 34728231 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Drayer’s syndrome of mental retardation, microcephaly, short stature and absent phalanges is caused by a recurrent deletion of chromosome 15(q26.2→qter). – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Rump%2C+P%2E%22">Rump, P.</searchLink><relatesTo>1</relatesTo><i> p.rump@medgen.umcg.nl</i><br /><searchLink fieldCode="AR" term="%22Dijkhuizen%2C+T%2E%22">Dijkhuizen, T.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Sikkema-Raddatz%2C+B%2E%22">Sikkema-Raddatz, B.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Lemmink%2C+H%2E+H%2E%22">Lemmink, H. H.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Vos%2C+Y%2E+J%2E%22">Vos, Y. J.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Verheij%2C+J%2E+B%2E+G%2E+M%2E%22">Verheij, J. B. G. M.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Van+Ravenswaaij%2C+C%2E+M%2E+A%2E%22">Van Ravenswaaij, C. M. A.</searchLink><relatesTo>1</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Clinical+Genetics%22">Clinical Genetics</searchLink>. Nov2008, Vol. 74 Issue 5, p455-462. 8p. 3 Black and White Photographs, 1 Diagram, 1 Chart, 1 Graph. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=34728231 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/j.1399-0004.2008.01064.x Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 8 StartPage: 455 Titles: – TitleFull: Drayer’s syndrome of mental retardation, microcephaly, short stature and absent phalanges is caused by a recurrent deletion of chromosome 15(q26.2→qter). Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Rump, P. – PersonEntity: Name: NameFull: Dijkhuizen, T. – PersonEntity: Name: NameFull: Sikkema-Raddatz, B. – PersonEntity: Name: NameFull: Lemmink, H. H. – PersonEntity: Name: NameFull: Vos, Y. J. – PersonEntity: Name: NameFull: Verheij, J. B. G. M. – PersonEntity: Name: NameFull: Van Ravenswaaij, C. M. A. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 11 Text: Nov2008 Type: published Y: 2008 Identifiers: – Type: issn-print Value: 00099163 Numbering: – Type: volume Value: 74 – Type: issue Value: 5 Titles: – TitleFull: Clinical Genetics Type: main |
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