Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants.
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| Title: | Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants. |
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| Authors: | Frisk, Sofia1,2 (AUTHOR), Wachtmeister, Alexandra1 (AUTHOR), Laurell, Tobias1,3 (AUTHOR), Lindstrand, Anna1,2 (AUTHOR), Jäntti, Nina1,2 (AUTHOR), Malmgren, Helena1,2 (AUTHOR), Lagerstedt‐Robinson, Kristina1,2 (AUTHOR), Tesi, Bianca1,2 (AUTHOR), Taylan, Fulya1,2 (AUTHOR), Nordgren, Ann1,2 (AUTHOR) ann.nordgren@ki.se |
| Source: | Molecular Genetics & Genomic Medicine. Apr2022, Vol. 10 Issue 4, p1-12. 12p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 156251867 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Frisk%2C+Sofia%22">Frisk, Sofia</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wachtmeister%2C+Alexandra%22">Wachtmeister, Alexandra</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Laurell%2C+Tobias%22">Laurell, Tobias</searchLink><relatesTo>1,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lindstrand%2C+Anna%22">Lindstrand, Anna</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jäntti%2C+Nina%22">Jäntti, Nina</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Malmgren%2C+Helena%22">Malmgren, Helena</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lagerstedt‐Robinson%2C+Kristina%22">Lagerstedt‐Robinson, Kristina</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Tesi%2C+Bianca%22">Tesi, Bianca</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Taylan%2C+Fulya%22">Taylan, Fulya</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Nordgren%2C+Ann%22">Nordgren, Ann</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> ann.nordgren@ki.se</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Molecular+Genetics+%26+Genomic+Medicine%22">Molecular Genetics & Genomic Medicine</searchLink>. Apr2022, Vol. 10 Issue 4, p1-12. 12p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=156251867 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/mgg3.1880 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 12 StartPage: 1 Titles: – TitleFull: Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Frisk, Sofia – PersonEntity: Name: NameFull: Wachtmeister, Alexandra – PersonEntity: Name: NameFull: Laurell, Tobias – PersonEntity: Name: NameFull: Lindstrand, Anna – PersonEntity: Name: NameFull: Jäntti, Nina – PersonEntity: Name: NameFull: Malmgren, Helena – PersonEntity: Name: NameFull: Lagerstedt‐Robinson, Kristina – PersonEntity: Name: NameFull: Tesi, Bianca – PersonEntity: Name: NameFull: Taylan, Fulya – PersonEntity: Name: NameFull: Nordgren, Ann IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 04 Text: Apr2022 Type: published Y: 2022 Identifiers: – Type: issn-print Value: 23249269 Numbering: – Type: volume Value: 10 – Type: issue Value: 4 Titles: – TitleFull: Molecular Genetics & Genomic Medicine Type: main |
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