A Turner syndrome neurocognitive phenotype maps to Xp22.3. - Wikidata - wikimedia - TriplyDB

A Turner syndrome neurocognitive phenotype maps to Xp22.3.

A Turner syndrome neurocognitive phenotype maps to Xp22.3.

http://www.wikidata.org/entity/Q34579701

about

Bone Fragility in Turner Syndrome: Mechanisms and Prevention Strategies Mouse model systems to study sex chromosome genes and behavior: relevance to humans.Cortical anatomy in human X monosomy Reversible histone methylation regulates brain gene expression and behavior.Cognitive profile of Turner syndrome.Genes that escape from X inactivation.The influence of sex-linked genetic mechanisms on attention and impulsivity.Turner syndrome and sexual differentiation of the brain: implications for understanding male-biased neurodevelopmental disorders Elucidating X chromosome influences on Attention Deficit Hyperactivity Disorder and executive function.Genomic sister-disorders of neurodevelopment: an evolutionary approach Accurate phenotyping: Reconciling approaches through Bayesian model averaging.X-chromosome inactivation and escape.Genomic imprinting effects of the X chromosome on brain morphology.Recombinant human growth hormone in the treatment of Turner syndrome.Sex chromosome-wide association analysis suggested male-specific risk genes for alcohol dependence.Pregnancy and cardiovascular risk for women with Turner syndrome.Attention deficit hyperactivity disorder (ADHD) in phenotypically similar neurogenetic conditions: Turner syndrome and the RASopathies Contribution of executive functions to visuospatial difficulties in prepubertal girls with Turner syndrome.Muscle function in Turner syndrome: normal force but decreased power.Recent Developments in Diagnosis and Care for Girls in Turner Syndrome

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A Turner syndrome neurocognitive phenotype maps to Xp22.3.

http://www.wikidata.org/entity/Q34579701

description

2007 nî lūn-bûn

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2007 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2007 թվականի մայիսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

A Turner syndrome neurocognitive phenotype maps to Xp22.3.

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A Turner syndrome neurocognitive phenotype maps to Xp22.3.

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A Turner syndrome neurocognitive phenotype maps to Xp22.3.

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A Turner syndrome neurocognitive phenotype maps to Xp22.3.

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A Turner syndrome neurocognitive phenotype maps to Xp22.3.

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A Turner syndrome neurocognitive phenotype maps to Xp22.3.

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A Turner syndrome neurocognitive phenotype maps to Xp22.3.

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A Turner syndrome neurocognitive phenotype maps to Xp22.3.

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A Turner syndrome neurocognitive phenotype maps to Xp22.3.

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Behavioral and Brain Functions

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A Turner syndrome neurocognitive phenotype maps to Xp22.3.

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David Roeltgen

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Frederick F Elder

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Gerry Stefanatos

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Harvey Kushner

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Judith L Ross

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Karen Kowal

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Purita Ramos

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The DNA sequence of the human X chromosome

A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins

X-inactivation profile reveals extensive variability in X-linked gene expression in females

A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation

Disorder-associated mutations lead to functional inactivation of neuroligins

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

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

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10.1186/1744-9081-3-24

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