3p14 deletion is a rare contiguous gene syndrome: Report of 2 new patients and an overview of 14 patients.
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| Title: | 3p14 deletion is a rare contiguous gene syndrome: Report of 2 new patients and an overview of 14 patients. |
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| Authors: | Dimitrov, B. I.1, Ogilvie, C.2, Wieczorek, D.3, Wakeling, E.4, Sikkema‐Raddatz, B.5, van Ravenswaaij‐Arts, C. M. A.5, Josifova, D.1 |
| Source: | American Journal of Medical Genetics. Part A; Jun2015, Vol. 167A Issue 6, p1223-1230, 8p |
| Database: | Applied Science & Technology Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: aci DbLabel: Applied Science & Technology Source An: 102899292 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=aci&AN=102899292 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.36556 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 8 StartPage: 1223 Titles: – TitleFull: 3p14 deletion is a rare contiguous gene syndrome: Report of 2 new patients and an overview of 14 patients. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Dimitrov, B. I. – PersonEntity: Name: NameFull: Ogilvie, C. – PersonEntity: Name: NameFull: Wieczorek, D. – PersonEntity: Name: NameFull: Wakeling, E. – PersonEntity: Name: NameFull: Sikkema‐Raddatz, B. – PersonEntity: Name: NameFull: van Ravenswaaij‐Arts, C. M. A. – PersonEntity: Name: NameFull: Josifova, D. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: Jun2015 Type: published Y: 2015 Identifiers: – Type: issn-print Value: 15524825 Numbering: – Type: volume Value: 167A – Type: issue Value: 6 Titles: – TitleFull: American Journal of Medical Genetics. Part A Type: main |
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