Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2040-2392
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features ; volume:10 ; number:1 ; day:3 ; month:5 ; year:2019 ; pages:1-13 ; date:12.2019
Molecular autism ; 10, Heft 1 (3.5.2019), 1-13, 12.2019
- Classification
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Medizin, Gesundheit
- Creator
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Baker, Emma K.
Arpone, Marta
Aliaga, Solange M.
Bretherton, Lesley
Kraan, Claudine M.
Bui, Minh
Slater, Howard R.
Ling, Ling
Francis, David
Hunter, Matthew F.
Elliott, Justine
Rogers, Carolyn
Field, Michael
Cohen, Jonathan
Cornish, Kim
Santa Maria, Lorena
Faundes, Victor
Curotto, Bianca
Morales, Paulina
Trigo, Cesar
Salas, Isabel
Alliende, Angelica M.
Amor, David J.
Godler, David E.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13229-019-0271-7
- URN
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urn:nbn:de:101:1-2019052702295885584861
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:51 AM CEST
Data provider
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Baker, Emma K.
- Arpone, Marta
- Aliaga, Solange M.
- Bretherton, Lesley
- Kraan, Claudine M.
- Bui, Minh
- Slater, Howard R.
- Ling, Ling
- Francis, David
- Hunter, Matthew F.
- Elliott, Justine
- Rogers, Carolyn
- Field, Michael
- Cohen, Jonathan
- Cornish, Kim
- Santa Maria, Lorena
- Faundes, Victor
- Curotto, Bianca
- Morales, Paulina
- Trigo, Cesar
- Salas, Isabel
- Alliende, Angelica M.
- Amor, David J.
- Godler, David E.
- SpringerLink (Online service)