Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A.
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| Title: | Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A. |
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| Authors: | Golas, Monika M.1, golas.monika@mh-hannover.de, Auber, Bernd1, Ripperger, Tim1, Pabst, Brigitte1, Schmidt, Gunnar1, Morlot, Michel2, Diebold, Uta3, Steinemann, Doris1, Schlegelberger, Brigitte1, Morlot, Susanne1 |
| Source: | American Journal of Medical Genetics. Part A; Jul2019, Vol. 179 Issue 7, p1383-1389, 7p |
| Database: | Applied Science & Technology Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: aci DbLabel: Applied Science & Technology Source An: 137027781 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Golas%2C+Monika+M%2E%22">Golas, Monika M.</searchLink><relatesTo>1</relatesTo>, <i>golas.monika@mh-hannover.de</i><br /><searchLink fieldCode="AU" term="%22Auber%2C+Bernd%22">Auber, Bernd</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Ripperger%2C+Tim%22">Ripperger, Tim</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Pabst%2C+Brigitte%22">Pabst, Brigitte</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Schmidt%2C+Gunnar%22">Schmidt, Gunnar</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Morlot%2C+Michel%22">Morlot, Michel</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AU" term="%22Diebold%2C+Uta%22">Diebold, Uta</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AU" term="%22Steinemann%2C+Doris%22">Steinemann, Doris</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Schlegelberger%2C+Brigitte%22">Schlegelberger, Brigitte</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Morlot%2C+Susanne%22">Morlot, Susanne</searchLink><relatesTo>1</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22American+Journal+of+Medical+Genetics%2E+Part+A%22">American Journal of Medical Genetics. Part A</searchLink>; Jul2019, Vol. 179 Issue 7, p1383-1389, 7p |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=aci&AN=137027781 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.61166 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 1383 Titles: – TitleFull: Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Golas, Monika M. – PersonEntity: Name: NameFull: Auber, Bernd – PersonEntity: Name: NameFull: Ripperger, Tim – PersonEntity: Name: NameFull: Pabst, Brigitte – PersonEntity: Name: NameFull: Schmidt, Gunnar – PersonEntity: Name: NameFull: Morlot, Michel – PersonEntity: Name: NameFull: Diebold, Uta – PersonEntity: Name: NameFull: Steinemann, Doris – PersonEntity: Name: NameFull: Schlegelberger, Brigitte – PersonEntity: Name: NameFull: Morlot, Susanne IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: Jul2019 Type: published Y: 2019 Identifiers: – Type: issn-print Value: 15524825 Numbering: – Type: volume Value: 179 – Type: issue Value: 7 Titles: – TitleFull: American Journal of Medical Genetics. Part A Type: main |
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