Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features

Location
Deutsche Nationalbibliothek Frankfurt am Main
ISSN
2040-2392
Extent
Online-Ressource
Language
Englisch
Notes
online resource.

Bibliographic citation
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
Medizin, Gesundheit

Creator
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
SpringerLink (Online service)

DOI
10.1186/s13229-019-0271-7
URN
urn:nbn:de:101:1-2019052702295885584861
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:51 AM CEST

Data provider

This object is provided by:
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)

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