Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.
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| Title: | Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program. |
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| Authors: | Jarmolowicz, Anna I.1, anna.jarmolowicz@mcri.edu.au, Baker, Emma K.2,3,4, Bartlett, Essra1, Francis, David1, Ling, Ling2, Gamage, Dinusha2, Delatycki, Martin B.1,3, Godler, David E.2,3 |
| Source: | American Journal of Medical Genetics. Part A; May2021, Vol. 185 Issue 5, p1498-1503, 6p |
| Database: | Applied Science & Technology Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: aci DbLabel: Applied Science & Technology Source An: 149731006 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Jarmolowicz%2C+Anna+I%2E%22">Jarmolowicz, Anna I.</searchLink><relatesTo>1</relatesTo>, <i>anna.jarmolowicz@mcri.edu.au</i><br /><searchLink fieldCode="AU" term="%22Baker%2C+Emma+K%2E%22">Baker, Emma K.</searchLink><relatesTo>2,3,4</relatesTo><br /><searchLink fieldCode="AU" term="%22Bartlett%2C+Essra%22">Bartlett, Essra</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Francis%2C+David%22">Francis, David</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AU" term="%22Ling%2C+Ling%22">Ling, Ling</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AU" term="%22Gamage%2C+Dinusha%22">Gamage, Dinusha</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AU" term="%22Delatycki%2C+Martin+B%2E%22">Delatycki, Martin B.</searchLink><relatesTo>1,3</relatesTo><br /><searchLink fieldCode="AU" term="%22Godler%2C+David+E%2E%22">Godler, David E.</searchLink><relatesTo>2,3</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>; May2021, Vol. 185 Issue 5, p1498-1503, 6p |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=aci&AN=149731006 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.62106 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 6 StartPage: 1498 Titles: – TitleFull: Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Jarmolowicz, Anna I. – PersonEntity: Name: NameFull: Baker, Emma K. – PersonEntity: Name: NameFull: Bartlett, Essra – PersonEntity: Name: NameFull: Francis, David – PersonEntity: Name: NameFull: Ling, Ling – PersonEntity: Name: NameFull: Gamage, Dinusha – PersonEntity: Name: NameFull: Delatycki, Martin B. – PersonEntity: Name: NameFull: Godler, David E. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: May2021 Type: published Y: 2021 Identifiers: – Type: issn-print Value: 15524825 Numbering: – Type: volume Value: 185 – Type: issue Value: 5 Titles: – TitleFull: American Journal of Medical Genetics. Part A Type: main |
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