1. Additional file 1: of Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features
- Author
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Baker, Emma, Arpone, Marta, Aliaga, Solange, Bretherton, Lesley, Kraan, Claudine, Bui, Minh, Slater, Howard, Ling, Ling, Francis, David, Hunter, Matthew, Elliott, Justine, Rogers, Carolyn, Field, Michael, Cohen, Jonathan, Cornish, Kim, Maria, Lorena Santa, Faundes, Victor, Curotto, Bianca, Morales, Paulina, Trigo, Cesar, Salas, Isabel, Alliende, Angelica, Amor, David, and Godler, David
- Subjects
congenital, hereditary, and neonatal diseases and abnormalities ,nervous system diseases - Abstract
Table S1. Comparison between males and females intellectual functioning (standard) scores. Table S2. Comparison between FM-only males with complete and incomplete FMR1 mRNA silencing on intellectual functioning (corrected) scores and autism features. Table S3. Relationship between intellectual functioning (standard) scores and FMR1 mRNA in males and females. Table S4. Relationship between intellectual functioning scores (corrected) and FMR1 mRNA in males and females with WISC-III (Chile) and MSEL removed. Table S5. Relationship between intellectual functioning (standard) scores with FMR1 mRNA in FM-only males with incomplete FMR1 mRNA silencing and PM/FM mosaic males. (DOCX 27 kb)
- Published
- 2019
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