Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review
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Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant womenDosage effects of X and Y chromosomes on language and social functioning in children with supernumerary sex chromosome aneuploidies: implications for idiopathic language impairment and autism spectrum disorders.Which neurodevelopmental disorders get researched and why?Mouse model systems to study sex chromosome genes and behavior: relevance to humans.The Sex Chromosome Trisomy mouse model of XXY and XYY: metabolism and motor performance.The psychiatric phenotype in triple X syndrome: new hypotheses illustrated in two casesA qualitative exploration of mothers' and fathers' experiences of having a child with Klinefelter syndrome and the process of reaching this diagnosis.Children with sex chromosome trisomies: parental disclosure of genetic status.Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencingThe psychosocial impact of Klinefelter syndrome and factors influencing quality of life.Monogenic and chromosomal causes of isolated speech and language impairment.Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies.Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancyA case-control study of brain structure and behavioral characteristics in 47,XXX syndrome.The phenotype of recurrent 10q22q23 deletions and duplications.Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexiaKlinefelter syndrome as a window on the aetiology of language and communication impairments in children: the neuroligin-neurexin hypothesis.Autism, language and communication in children with sex chromosome trisomies.The influence of sex-linked genetic mechanisms on attention and impulsivity.Sex chromosomes and the brain: a study of neuroanatomy in XYY syndromeThe eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy.Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYYBehavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndromeEveryday executive functions in Down syndrome from early childhood to young adulthood: evidence for both unique and shared characteristics compared to youth with sex chromosome trisomy (XXX and XXY).Commentary: Unravelling the effects of additional sex chromosomes on cognition and communication--reflections on Lee et al. (2012).Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior.Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features.The spectrum of the behavioral phenotype in boys and adolescents 47,XXY (Klinefelter syndrome).Neural systems for social cognition: gray matter volume abnormalities in boys at high genetic risk of autism symptoms, and a comparison with idiopathic autism spectrum disorderSocial attention, affective arousal and empathy in men with Klinefelter syndrome (47,XXY): evidence from eyetracking and skin conductance.Factors associated with adaptation to Klinefelter syndrome: the experience of adolescents and adults.Brain morphology in children with 47, XYY syndrome: a voxel- and surface-based morphometric study.Postnatal screening for Klinefelter syndrome: is there a rationale?Neurocognitive variance and neurological underpinnings of the X and Y chromosomal variations.Autism spectrum disorders in XYY syndrome: two new cases and systematic review of the literature.Annual research review: Rare genotypes and childhood psychopathology--uncovering diverse developmental mechanisms of ADHD risk.Sleep Problems and Life Satisfaction as Predictors of Health in Men with Sex Chromosome Aneuploidies.Advances in the Interdisciplinary Care of Children with Klinefelter Syndrome.The benefits and limitations of cell-free DNA screening for 47, XXY (Klinefelter syndrome).Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study.
P2860
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P2860
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review
description
2010 nî lūn-bûn
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2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Neurocognitive outcomes of ind ...... Y, or XXY: a systematic review
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Neurocognitive outcomes of ind ...... Y, or XXY: a systematic review
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Neurocognitive outcomes of ind ...... Y, or XXY: a systematic review
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type
label
Neurocognitive outcomes of ind ...... Y, or XXY: a systematic review
@ast
Neurocognitive outcomes of ind ...... Y, or XXY: a systematic review
@en
Neurocognitive outcomes of ind ...... Y, or XXY: a systematic review
@nl
prefLabel
Neurocognitive outcomes of ind ...... Y, or XXY: a systematic review
@ast
Neurocognitive outcomes of ind ...... Y, or XXY: a systematic review
@en
Neurocognitive outcomes of ind ...... Y, or XXY: a systematic review
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P2093
P2860
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Neurocognitive outcomes of ind ...... Y, or XXY: a systematic review
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P2093
Dorothy V M Bishop
Gaia Scerif
Victoria Leggett
P2860
P304
P3181
P356
10.1111/J.1469-8749.2009.03545.X
P407
P5008
P577
2010-02-01T00:00:00Z