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Publications by Emma K. Baker
Incomplete Silencing of Full Mutation Alleles in Males With Fragile X Syndrome Is Associated With Autistic Features
Molecular Autism
Psychiatry
Mental Health
Developmental Neuroscience
Developmental Biology
Molecular Biology
Exploring Autism Symptoms in an Australian Cohort of Patients With Prader-Willi and Angelman Syndromes
Journal of Neurodevelopmental Disorders
Pediatrics
Cognitive Neuroscience
Perinatology
Neurology
Forensic Medicine
Child Health
Pathology
Related publications
Hypertension inFMR1premutation Males With and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)
American Journal of Medical Genetics, Part A
Genetics
Electrocortical Changes Associated With Minocycline Treatment in Fragile X Syndrome
Journal of Psychopharmacology
Medicine
Psychiatry
Mental Health
Pharmacology
Frequency of the Fragile X Syndrome in Japanese Mentally Retarded Males
Human Genetics
Genetics
Finiteness Marking in Boys With Fragile X Syndrome
Journal of Speech, Language, and Hearing Research
Medicine
Linguistics
Speech
Language
Hearing
Dementia in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Comparison With Alzheimer's Disease
American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics
Psychiatry
Molecular Neuroscience
Mental Health
Genetics
Cellular
Mouse Models of the Fragile X Premutation and the Fragile X Associated Tremor/Ataxia Syndrome
Results and Problems in Cell Differentiation
Developmental Biology
Cell Biology
Expansion of the Fragile X CGG Repeat in Females With Premutation or Intermediate Alleles
American Journal of Human Genetics
Genetics
Fragile X Syndrome
Journal of the Royal Society of Medicine
Medicine
Fragile X Syndrome
