Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder - Test2 - elhamkhani - TriplyDB

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

http://www.wikidata.org/entity/Q24801230

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Genetics evaluation for the etiologic diagnosis of autism spectrum disorders The genetics of autistic disorders and its clinical relevance: a review of the literature Intranasal oxytocin for autism spectrum disorders (ASD)Genetics of autistic disorders: review and clinical implications Clinical Genetic Aspects of ASD Spectrum Disorders Fragile X: leading the way for targeted treatments in autism.Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.Heterogeneity within Autism Spectrum Disorders: What have We Learned from Neuroimaging Studies?Molecular cytogenetics and cytogenomics of brain diseases.Broad clinical involvement in a family affected by the fragile X premutation.Dynamic Object Representations in Infants with and without Fragile X Syndrome.Gene × Environment interactions in autism spectrum disorders: role of epigenetic mechanisms.Identification of expanded alleles of the FMR1 gene among high-risk population in Indonesia by using blood spot screening Haploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems.Phonological processing in first-degree relatives of individuals with autism: an fMRI study.Genetic studies in children with intellectual disability and autistic spectrum of disorders.Genetics of autism and mental retardation: A spoonful from the sea!Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.Fragile X and autism: Intertwined at the molecular level leading to targeted treatments.The dwarf phenotype in GH240B mice, haploinsufficient for the autism candidate gene Neurobeachin, is caused by ectopic expression of recombinant human growth hormone.Somatic genome variations in health and disease Fragile X syndrome: clinical, cytogenetic and molecular screening among autism spectrum disorder children in Indonesia.Clinical genetic testing for patients with autism spectrum disorders Autism-lessons from the X chromosome.Clinical genetics evaluation in identifying the etiology of autism spectrum disorders.The ongoing dissection of the genetic architecture of autistic spectrum disorder Fragile X syndrome screening in Chinese children with unknown intellectual developmental disorder.Cut-like homeobox 1 and nuclear factor I/B mediate ENGRAILED2 autism spectrum disorder-associated haplotype function.A Case of Autism with Ring Chromosome 14.Quantitation of melatonin and n-acetylserotonin in human plasma by nanoflow LC-MS/MS and electrospray LC-MS/MS.Nuclear Localization of the Autism Candidate Gene Neurobeachin and Functional Interaction with the NOTCH1 Intracellular Domain Indicate a Role in Regulating Transcription.Genetic testing in children with autism spectrum disorders.Autism spectrum disorders: from genes to neurobiology Identification of expanded alleles of the FMR1 Gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study.Fragile X Syndrome: Scientific Background and Screening Technologies.High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism.Using infrared eye-tracking to explore ordinal numerical processing in toddlers with Fragile X Syndrome Plasma cytokine profiles in Fragile X subjects: is there a role for cytokines in the pathogenesis?The genomically mosaic brain: aneuploidy and more in neural diversity and disease.

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Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

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Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

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Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

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Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

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Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

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Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

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Kavita S Reddy

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Genetics of austim: complex aetiology for a heterogeneous disorder

Pervasive Developmental Disorders in Preschool Children

The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

Altered synaptic plasticity in a mouse model of fragile X mental retardation

A genomewide screen of 345 families for autism-susceptibility loci.

The fragile-X premutation: a maturing perspective.

A genomic screen of autism: evidence for a multilocus etiology.

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

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Autism spectrum

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