Pages that link to "Q50312686"
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The following pages link to The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: a family history study (Q50312686):
Displaying 50 items.
- The genetics of autistic disorders and its clinical relevance: a review of the literature (Q22250987) (← links)
- The ‘Fractionable Autism Triad’: A Review of Evidence from Behavioural, Genetic, Cognitive and Neural Research (Q22252620) (← links)
- Asperger syndrome (Q22252681) (← links)
- Current developments in the genetics of autism: from phenome to genome (Q24646514) (← links)
- Out of the mouths of babes: vocal production in infant siblings of children with ASD (Q30468081) (← links)
- Common genetic variants, acting additively, are a major source of risk for autism (Q30536405) (← links)
- Heterogeneity of subclinical autistic traits among parents of children with autism spectrum disorder: Identifying the broader autism phenotype with a data-driven method. (Q31112787) (← links)
- Genetic and Neurodevelopmental Influences in Autistic Disorder (Q33194174) (← links)
- A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples (Q33556118) (← links)
- Language and reading abilities of children with autism spectrum disorders and specific language impairment and their first-degree relatives (Q33589916) (← links)
- Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome (Q33622905) (← links)
- Familial aggregation of quantitative autistic traits in multiplex versus simplex autism (Q33642648) (← links)
- Dynamic infant-parent affect coupling during the face-to-face/still-face (Q33802073) (← links)
- The classification of autism, Asperger's syndrome, and pervasive developmental disorder (Q33925850) (← links)
- Cognitive profiles and social-communicative functioning in children with autism spectrum disorder (Q33947562) (← links)
- Verbal and spatial working memory in autism (Q33991227) (← links)
- Predicting social impairment and ASD diagnosis in younger siblings of children with autism spectrum disorder (Q34061219) (← links)
- Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment (Q34293550) (← links)
- A review of the role of female gender in autism spectrum disorders. (Q34335090) (← links)
- Social demographic change and autism (Q34395694) (← links)
- Neurodevelopmental disorders: cluster 2 of the proposed meta-structure for DSM-V and ICD-11. (Q34427739) (← links)
- The genetic relationship between individual differences in social and nonsocial behaviours characteristic of autism (Q34437542) (← links)
- Physiologic Arousal to Social Stress in Children with Autism Spectrum Disorders: A Pilot Study (Q35539205) (← links)
- Evidence for broader autism phenotype characteristics in parents from multiple-incidence autism families (Q35613003) (← links)
- Conducting genetic epidemiology studies of autism spectrum disorders: issues in matching (Q35751636) (← links)
- The broader autism phenotype and its implications on the etiology and treatment of autism spectrum disorders (Q36168469) (← links)
- New Interview and Observation Measures of the Broader Autism Phenotype: Description of Strategy and Reliability Findings for the Interview Measures (Q36401544) (← links)
- Quantitative autistic traits ascertained in a national survey of 22 529 Japanese schoolchildren (Q36704130) (← links)
- Peripheral blood gene expression signature differentiates children with autism from unaffected siblings. (Q36939583) (← links)
- Episodic memory retrieval for story characters in high-functioning autism (Q36964609) (← links)
- Sex differences and within-family associations in the broad autism phenotype (Q36988894) (← links)
- A molecular genetic study of autism and related phenotypes in extended pedigrees (Q37364504) (← links)
- Parental broader autism subphenotypes in ASD affected families: relationship to gender, child's symptoms, SSRI treatment, and platelet serotonin. (Q37407569) (← links)
- Increased Sensory Processing Atypicalities in Parents of Multiplex ASD Families Versus Typically Developing and Simplex ASD Families. (Q37703239) (← links)
- Autistic traits below the clinical threshold: re-examining the broader autism phenotype in the 21st century (Q37944510) (← links)
- The Broader Autism Phenotype in Mothers is Associated with Increased Discordance Between Maternal-Reported and Clinician-Observed Instruments that Measure Child Autism Spectrum Disorder (Q38658535) (← links)
- Matching procedures in autism research: evidence from meta-analytic studies (Q40516036) (← links)
- Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families (Q42559323) (← links)
- Genetically determined low maternal serum dopamine beta-hydroxylase levels and the etiology of autism spectrum disorders (Q43598045) (← links)
- Sex differences in toddlers with autism spectrum disorders (Q43858908) (← links)
- The broader autism phenotype in simplex and multiplex families (Q44284728) (← links)
- Clinical assessment of autism in high-risk 18-month-olds (Q44565978) (← links)
- Atypical sleep architecture and the autism phenotype (Q45261090) (← links)
- Brief report: do the nature of communication impairments in autism spectrum disorders relate to the broader autism phenotype in parents? (Q45909003) (← links)
- Predictors of psychiatric symptoms in children with an autism spectrum disorder (Q48354453) (← links)
- Autistic-like traits and their association with mental health problems in two nationwide twin cohorts of children and adults (Q48887762) (← links)
- Brief Report: Autism Symptoms in Infants with Fragile X Syndrome (Q50301305) (← links)
- Communicative competence in parents of children with autism and parents of children with specific language impairment (Q50302014) (← links)
- Studying the emergence of autism spectrum disorders in high-risk infants: methodological and practical issues (Q50303220) (← links)
- Parent-reported patterns of loss and gain in communication in 1- to 2-year-old children are not unique to autism spectrum disorder. (Q50304237) (← links)