A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the SAMD9 Gene.
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| Title: | A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the SAMD9 Gene. |
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| Authors: | Mengen, Eda1 drmengen@hotmail.com, Yavaş, Aynur Küçükçongar2, Uçaktürk, S. Ahmet1 |
| Source: | Journal of Clinical Research in Pediatric Endocrinology. Jun2020, Vol. 12 Issue 2, p206-211. 6p. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 143647626 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=143647626 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.4274/jcrpe.galenos.2019.2019.0053 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 6 StartPage: 206 Titles: – TitleFull: A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the SAMD9 Gene. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Mengen, Eda – PersonEntity: Name: NameFull: Yavaş, Aynur Küçükçongar – PersonEntity: Name: NameFull: Uçaktürk, S. Ahmet IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: Jun2020 Type: published Y: 2020 Identifiers: – Type: issn-print Value: 13085727 Numbering: – Type: volume Value: 12 – Type: issue Value: 2 Titles: – TitleFull: Journal of Clinical Research in Pediatric Endocrinology Type: main |
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