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

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Title: Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.
Authors: Baker, Emma K.1,2 (AUTHOR) emma.baker@mcri.edu.au, Arpone, Marta1,2,3 (AUTHOR) marta.arpone@mcri.edu.au, Aliaga, Solange M.1 (AUTHOR) solange.aliagavera@mcri.edu.au, Bretherton, Lesley3 (AUTHOR) Lesley.Bretherton@mcri.edu.au, Kraan, Claudine M.1,2 (AUTHOR) claudine.kraan@mcri.edu.au, Bui, Minh4 (AUTHOR) mbui@unimelb.edu.au, Slater, Howard R.1 (AUTHOR) howard.slater@vcgs.org.au, Ling, Ling1 (AUTHOR) ling.ling@mcri.edu.au, Francis, David5 (AUTHOR) david.francis@vcgs.org.au, Hunter, Matthew F.6,7 (AUTHOR) Matthew.Hunter@monashhealth.org, Elliott, Justine5 (AUTHOR) justine.elliott@vcgs.org.au, Rogers, Carolyn8 (AUTHOR) carolyn.rogers@health.nsw.gov.au, Field, Michael8 (AUTHOR) Mike.Field@health.nsw.gov.au, Cohen, Jonathan9 (AUTHOR) jcohen@geneticclinic.com.au, Cornish, Kim10 (AUTHOR) Kim.Cornish@monash.edu, Santa Maria, Lorena11 (AUTHOR) lsantamaria@inta.uchile.cl, Faundes, Victor11 (AUTHOR) vfaundes@inta.uchile.cl, Curotto, Bianca11 (AUTHOR) bcurotto@inta.uchile.cl, Morales, Paulina11 (AUTHOR) pmorales@inta.uchile.cl, Trigo, Cesar11 (AUTHOR) catrigo@yahoo.com
Source: Molecular Autism. 5/3/2019, Vol. 10 Issue 1, pN.PAG-N.PAG. 1p.
Database: Academic Search Ultimate
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  Data: Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.
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  Data: <searchLink fieldCode="JN" term="%22Molecular+Autism%22">Molecular Autism</searchLink>. 5/3/2019, Vol. 10 Issue 1, pN.PAG-N.PAG. 1p.
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