Pages that link to "Q47336770"

The following pages link to Screening of the ARX gene in 682 retarded males. (Q47336770):

Displaying 27 items.

• Childhood autism and associated comorbidities (Q22252337) (← links)
• A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome) (Q24678062) (← links)
• XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene (Q24810185) (← links)
• Obtaining genetic testing in pediatric epilepsy (Q28082549) (← links)
• The c.429_452 duplication of the ARX gene: a unique developmental-model of limb kinetic apraxia (Q30577795) (← links)
• MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions (Q33283739) (← links)
• Regulation of histone H3K4 methylation in brain development and disease (Q34079415) (← links)
• Unraveling the pathogenesis of ARX polyalanine tract variants using a clinical and molecular interfacing approach (Q35648072) (← links)
• X linked mental retardation: a clinical guide (Q36239035) (← links)
• Mutation screening of the ARX gene in patients with autism (Q36783161) (← links)
• A novel mutation of the ARX gene in a male with nonsyndromic mental retardation. (Q36886749) (← links)
• Identification of Arx transcriptional targets in the developing basal forebrain (Q36967946) (← links)
• ARX spectrum disorders: making inroads into the molecular pathology (Q37761093) (← links)
• Genetics, molecular biology, and phenotypes of x-linked epilepsy (Q38164570) (← links)
• Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation. (Q42930411) (← links)
• Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations. (Q43804873) (← links)
• Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation (Q48332931) (← links)
• A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females (Q48887866) (← links)
• Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis (Q50123029) (← links)
• Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene (Q50311390) (← links)
• Mutational screening of ARX gene in Brazilian males with mental retardation of unknown etiology. (Q51914749) (← links)
• Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardation. (Q51927335) (← links)
• X-linked mental retardation (Q56270643) (← links)
• Wwox deletion leads to reduced GABA-ergic inhibitory interneuron numbers and activation of microglia and astrocytes in mouse hippocampus (Q57048955) (← links)
• ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia (Q57387330) (← links)
• Contractions in the second polyA tract of ARX are rare, non-pathogenic polymorphisms (Q57529907) (← links)
• A novel de novo 27 bp duplication of theARXgene, resulting from postzygotic mosaicism and leading to three severely affected males in two generations (Q57733973) (← links)