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4. Associations between Early Maternal Behaviours and Child Language at 36 Months in a Cohort Experiencing Adversity

6. Predictive Validity of Verbal and Non-Verbal Communication and Mother-Child Turn-Taking at 12 Months on Language Outcomes at 24 and 36 Months in a Cohort of Infants Experiencing Adversity: A Preliminary Study

9. Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

10. Parents' Experiences of Their Children's Supplementary Reading Intervention: A Qualitative Exploration

12. Developing a Comprehensive Model of Risk and Protective Factors That Can Predict Spelling at Age Seven: Findings from a Community Sample of Victorian Children

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

15. Stability of Language Performance at 4 and 5 Years: Measurement and Participant Variability

16. Developing Relationships between Language and Behaviour in Preschool Children from the Early Language in Victoria Study: Implications for Intervention

18. Children with Specific Language Impairment and Resolved Late Talkers: Working Memory Profiles at 5 Years

19. Assessing Early Communication Behaviours: Structure and Validity of the Communication and Symbolic Behaviour Scales-Developmental Profile (CSBS-DP) in 12-Month-Old Infants

20. The Relationship between Auditory Temporal Processing, Phonemic Awareness, and Reading Disability.

21. Prediction of clinical anxious and depressive problems in mid childhood amongst temperamentally inhibited preschool children: a population study

22. Follow‐up of the Cool Little Kids translational trial into middle childhood

23. Children with specific language impairment and resolved late talkers: working memory profiles at 5 years

26. DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome

30. Follow‐up of the Cool Little Kids translational trial into middle childhood.

31. Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing

32. Cool Little Kids translational trial to prevent internalising: two‐year outcomes and prediction of parent engagement.

33. Additional file 1: of Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features

40. Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X

46. Cohort Profile: The Early Language in Victoria Study (ELVS)

48. Erratum: Hwang Y.T. et al. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes 2016, 7, 68

49. Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: A case report

50. Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia

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