No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.
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| Title: | No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome. |
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| Authors: | Schlögel, Matthieu J.1, Mendola, Antonella1, Fastré, Elodie1, Vasudevan, Pradeep2, Devriendt, Koen3, de Ravel, Thomy J. L.3, Van Esch, Hilde3, Casteels, Ingele4, Arroyo Carrera, Ignacio5, Cristofoli, Francesca3, Fieggen, Karen6, Jones, Katheryn7, Lipson, Mark7, Balikova, Irina8, Singer, Ami9, Soller, Maria10, Villanueva, María Mercedes11, Revencu, Nicole1,12, Boon, Laurence M.1,13, Brouillard, Pascal1 |
| Source: | Orphanet Journal of Rare Diseases. Jun2015, Vol. 10 Issue 1, p1-11. 11p. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 108277543 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=asn&AN=108277543 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-015-0271-4 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 1 Titles: – TitleFull: No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Schlögel, Matthieu J. – PersonEntity: Name: NameFull: Mendola, Antonella – PersonEntity: Name: NameFull: Fastré, Elodie – PersonEntity: Name: NameFull: Vasudevan, Pradeep – PersonEntity: Name: NameFull: Devriendt, Koen – PersonEntity: Name: NameFull: de Ravel, Thomy J. L. – PersonEntity: Name: NameFull: Van Esch, Hilde – PersonEntity: Name: NameFull: Casteels, Ingele – PersonEntity: Name: NameFull: Arroyo Carrera, Ignacio – PersonEntity: Name: NameFull: Cristofoli, Francesca – PersonEntity: Name: NameFull: Fieggen, Karen – PersonEntity: Name: NameFull: Jones, Katheryn – PersonEntity: Name: NameFull: Lipson, Mark – PersonEntity: Name: NameFull: Balikova, Irina – PersonEntity: Name: NameFull: Singer, Ami – PersonEntity: Name: NameFull: Soller, Maria – PersonEntity: Name: NameFull: Villanueva, María Mercedes – PersonEntity: Name: NameFull: Revencu, Nicole – PersonEntity: Name: NameFull: Boon, Laurence M. – PersonEntity: Name: NameFull: Brouillard, Pascal IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: Jun2015 Type: published Y: 2015 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 10 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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