Fetal phenotypes in otopalatodigital spectrum disorders.
Saved in:
| Title: | Fetal phenotypes in otopalatodigital spectrum disorders. |
|---|---|
| Authors: | Naudion, S.1, Moutton, S.1,2, Coupry, I.2, Sole, G.2,3, Deforges, J.1, Guerineau, E.2, Hubert, C.4, Deves, S.1, Pilliod, J.2, Rooryck, C.1,2, Abel, C.5, Le Breton, F.6, Collardeau‐Frachon, S.7, Cordier, M.P.8, Delezoide, A.L.9, Goldenberg, A.10, Loget, P.11, Melki, J.12, Odent, S.13, Patrier, S.14 |
| Source: | Clinical Genetics. Mar2016, Vol. 89 Issue 3, p371-377. 7p. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| FullText | Links: – Type: pdflink Text: Availability: 1 |
|---|---|
| Header | DbId: asn DbLabel: Academic Search Ultimate An: 112965653 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Fetal phenotypes in otopalatodigital spectrum disorders. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Naudion%2C+S%2E%22">Naudion, S.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Moutton%2C+S%2E%22">Moutton, S.</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Coupry%2C+I%2E%22">Coupry, I.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Sole%2C+G%2E%22">Sole, G.</searchLink><relatesTo>2,3</relatesTo><br /><searchLink fieldCode="AR" term="%22Deforges%2C+J%2E%22">Deforges, J.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Guerineau%2C+E%2E%22">Guerineau, E.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Hubert%2C+C%2E%22">Hubert, C.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Deves%2C+S%2E%22">Deves, S.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Pilliod%2C+J%2E%22">Pilliod, J.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Rooryck%2C+C%2E%22">Rooryck, C.</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Abel%2C+C%2E%22">Abel, C.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Le+Breton%2C+F%2E%22">Le Breton, F.</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Collardeau‐Frachon%2C+S%2E%22">Collardeau‐Frachon, S.</searchLink><relatesTo>7</relatesTo><br /><searchLink fieldCode="AR" term="%22Cordier%2C+M%2EP%2E%22">Cordier, M.P.</searchLink><relatesTo>8</relatesTo><br /><searchLink fieldCode="AR" term="%22Delezoide%2C+A%2EL%2E%22">Delezoide, A.L.</searchLink><relatesTo>9</relatesTo><br /><searchLink fieldCode="AR" term="%22Goldenberg%2C+A%2E%22">Goldenberg, A.</searchLink><relatesTo>10</relatesTo><br /><searchLink fieldCode="AR" term="%22Loget%2C+P%2E%22">Loget, P.</searchLink><relatesTo>11</relatesTo><br /><searchLink fieldCode="AR" term="%22Melki%2C+J%2E%22">Melki, J.</searchLink><relatesTo>12</relatesTo><br /><searchLink fieldCode="AR" term="%22Odent%2C+S%2E%22">Odent, S.</searchLink><relatesTo>13</relatesTo><br /><searchLink fieldCode="AR" term="%22Patrier%2C+S%2E%22">Patrier, S.</searchLink><relatesTo>14</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Clinical+Genetics%22">Clinical Genetics</searchLink>. Mar2016, Vol. 89 Issue 3, p371-377. 7p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=112965653 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.12679 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 371 Titles: – TitleFull: Fetal phenotypes in otopalatodigital spectrum disorders. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Naudion, S. – PersonEntity: Name: NameFull: Moutton, S. – PersonEntity: Name: NameFull: Coupry, I. – PersonEntity: Name: NameFull: Sole, G. – PersonEntity: Name: NameFull: Deforges, J. – PersonEntity: Name: NameFull: Guerineau, E. – PersonEntity: Name: NameFull: Hubert, C. – PersonEntity: Name: NameFull: Deves, S. – PersonEntity: Name: NameFull: Pilliod, J. – PersonEntity: Name: NameFull: Rooryck, C. – PersonEntity: Name: NameFull: Abel, C. – PersonEntity: Name: NameFull: Le Breton, F. – PersonEntity: Name: NameFull: Collardeau‐Frachon, S. – PersonEntity: Name: NameFull: Cordier, M.P. – PersonEntity: Name: NameFull: Delezoide, A.L. – PersonEntity: Name: NameFull: Goldenberg, A. – PersonEntity: Name: NameFull: Loget, P. – PersonEntity: Name: NameFull: Melki, J. – PersonEntity: Name: NameFull: Odent, S. – PersonEntity: Name: NameFull: Patrier, S. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: Mar2016 Type: published Y: 2016 Identifiers: – Type: issn-print Value: 00099163 Numbering: – Type: volume Value: 89 – Type: issue Value: 3 Titles: – TitleFull: Clinical Genetics Type: main |
| ResultId | 1 |