Pages that link to "Q56270643"
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The following pages link to X-linked mental retardation (Q56270643):
Displaying 50 items.
- Estimating the inbreeding depression on cognitive behavior: a population based study of child cohort (Q21090586) (← links)
- Why are autism spectrum conditions more prevalent in males? (Q21145770) (← links)
- In-silico human genomics with GeneCards (Q21245450) (← links)
- Etiologies underlying sex differences in Autism Spectrum Disorders (Q22251432) (← links)
- Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic Epidemiology (Q24273406) (← links)
- Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation (Q24292830) (← links)
- The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases (Q24298299) (← links)
- A circadian clock in hippocampus is regulated by interaction between oligophrenin-1 and Rev-erbα (Q24336512) (← links)
- Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13 (Q24612956) (← links)
- A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation (Q24613870) (← links)
- Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature (Q24615911) (← links)
- Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation (Q24629491) (← links)
- A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate (Q24650497) (← links)
- Comparative genomics and molecular dynamics of DNA repeats in eukaryotes (Q24650948) (← links)
- Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation (Q24671723) (← links)
- UBE2A, which encodes a ubiquitin-conjugating enzyme, is mutated in a novel X-linked mental retardation syndrome (Q24678557) (← links)
- The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behavior (Q24680417) (← links)
- The role of neuronal complexes in human X-linked brain diseases (Q24680472) (← links)
- X chromosome cDNA microarray screening identifies a functional PLP2 promoter polymorphism enriched in patients with X-linked mental retardation (Q24681478) (← links)
- Advances in understanding - genetic basis of intellectual disability (Q26748977) (← links)
- SYNGAP1: Mind the Gap (Q26766506) (← links)
- Autism spectrum disorders and neuropathology of the cerebellum (Q26853603) (← links)
- Rab and Arf proteins in genetic diseases (Q26862704) (← links)
- Fragile X and X-linked intellectual disability: four decades of discovery (Q27027343) (← links)
- ATRX ADD domain links an atypical histone methylation recognition mechanism to human mental-retardation syndrome (Q27670417) (← links)
- X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes (Q28118573) (← links)
- HSD17B10: a gene involved in cognitive function through metabolism of isoleucine and neuroactive steroids (Q28235702) (← links)
- Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate (Q28238420) (← links)
- Genetic foundations of human intelligence (Q28238449) (← links)
- Histone H3K4 demethylases are essential in development and differentiation (Q28241709) (← links)
- The impact of genetic research on our understanding of normal cognitive ageing: 1995 to 2009 (Q28259199) (← links)
- Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor (Q28284058) (← links)
- Mutation in CUL4B, which encodes a member of cullin-RING ubiquitin ligase complex, causes X-linked mental retardation (Q28286574) (← links)
- Evolutionary genomics of human intellectual disability (Q28729961) (← links)
- Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability (Q29147451) (← links)
- Sex differences in protein expression in the mouse brain and their perturbations in a model of Down syndrome (Q30398962) (← links)
- Developmental vulnerability of synapses and circuits associated with neuropsychiatric disorders (Q30435763) (← links)
- An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity. (Q30448340) (← links)
- Event-related potential alterations in fragile X syndrome (Q30463379) (← links)
- MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions (Q33283739) (← links)
- Effects of sex chromosome aneuploidies on brain development: evidence from neuroimaging studies (Q33518807) (← links)
- Spatial Prevalence of Intellectual Disability and Related Socio-Demographic Factors in Iran, Using GWR: Case Study (2006) (Q33600881) (← links)
- Drosophila, a genetic model system to study cocaine-related behaviors: a review with focus on LIM-only proteins. (Q33642755) (← links)
- Phenotype ontologies for mouse and man: bridging the semantic gap. (Q33815395) (← links)
- Dosage compensation of the active X chromosome in mammals (Q33992021) (← links)
- Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation (Q34087624) (← links)
- Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene. (Q34160063) (← links)
- ST3GAL3 mutations impair the development of higher cognitive functions. (Q34215113) (← links)
- The genetic basis of non-syndromic intellectual disability: a review (Q34283901) (← links)
- Gene targeting study reveals unexpected expression of brain-expressed X-linked 2 in endocrine and tissue stem/progenitor cells in mice (Q34396905) (← links)