skip to main content
Idioma:
Resultados 1 2 next page
Mostrar Somente
Refinado por: xxx: xxx remover Child remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Vulnerability for autism traits in boys and men with an extra X chromosome (47,XXY): The mediating role of cognitive flexibility
Vulnerability for autism traits in boys and men with an extra X chromosome (47,XXY): The mediating role of cognitive flexibility
Material Type:
Artigo 		Adicionar ao Meu Espaço

Vulnerability for autism traits in boys and men with an extra X chromosome (47,XXY): The mediating role of cognitive flexibility

van Rijn, Sophie ; Bierman, Marit ; Bruining, Hilgo ; Swaab, Hanna

Journal of psychiatric research, 2012-10, Vol.46 (10), p.1300-1306 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

Texto completo disponível

Citações Citado por
2
Chromosomal Abnormalities in Patients With Autism Spectrum Disorders From Taiwan
Chromosomal Abnormalities in Patients With Autism Spectrum Disorders From Taiwan
Material Type:
Artigo 		Adicionar ao Meu Espaço

Chromosomal Abnormalities in Patients With Autism Spectrum Disorders From Taiwan

Liao, Hsiao-Mei ; Gau, Susan Shur-Fen ; Tsai, Wen-Che ; Fang, Jye-Siung ; Su, Ying-Cheng ; Chou, Miao-Chun ; Liu, Shih-Kai ; Chou, Wen-Jiun ; Wu, Yu-Yu ; Chen, Chia-Hsiang

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2013-10, Vol.162B (7), p.734-741 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
3
Social cognition and underlying cognitive mechanisms in children with an extra X chromosome: a comparison with autism spectrum disorder
Social cognition and underlying cognitive mechanisms in children with an extra X chromosome: a comparison with autism spectrum disorder
Material Type:
Artigo 		Adicionar ao Meu Espaço

Social cognition and underlying cognitive mechanisms in children with an extra X chromosome: a comparison with autism spectrum disorder

van Rijn, S. ; Stockmann, L. ; van Buggenhout, G. ; van Ravenswaaij‐Arts, C. ; Swaab, H.

Genes, brain and behavior, 2014-06, Vol.13 (5), p.459-467 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
4
Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features
Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features
Material Type:
Artigo 		Adicionar ao Meu Espaço

Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features

Ross, J. L. ; Tartaglia, N. ; Merry, D. E. ; Dalva, M. ; Zinn, A. R.

Genes, brain and behavior, 2015-02, Vol.14 (2), p.137-144 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
5
Annual Research Review: Rare genotypes and childhood psychopathology - uncovering diverse developmental mechanisms of ADHD risk
Annual Research Review: Rare genotypes and childhood psychopathology - uncovering diverse developmental mechanisms of ADHD risk
Material Type:
Artigo 		Adicionar ao Meu Espaço

Annual Research Review: Rare genotypes and childhood psychopathology - uncovering diverse developmental mechanisms of ADHD risk

Scerif, Gaia ; Baker, Kate

Journal of child psychology and psychiatry, 2015-03, Vol.56 (3), p.251-273 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
6
Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXX
Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXX
Material Type:
Artigo 		Adicionar ao Meu Espaço

Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXX

Samango-Sprouse, Carole ; Keen, Colleen ; Mitchell, Francie ; Sadeghin, Teresa ; Gropman, Andrea

American journal of medical genetics. Part A, 2015-10, Vol.167A (10), p.2251-2259 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
7
Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis
Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis

Wigby, Kristen ; D'Epagnier, Cheryl ; Howell, Susan ; Reicks, Amy ; Wilson, Rebecca ; Cordeiro, Lisa ; Tartaglia, Nicole

American journal of medical genetics. Part A, 2016-11, Vol.170A (11), p.2870-2881 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
8
Characterization of autism spectrum disorder and neurodevelopmental profiles in youth with XYY syndrome
Characterization of autism spectrum disorder and neurodevelopmental profiles in youth with XYY syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Characterization of autism spectrum disorder and neurodevelopmental profiles in youth with XYY syndrome

Joseph, Lisa ; Farmer, Cristan ; Chlebowski, Colby ; Henry, Laura ; Fish, Ari ; Mankiw, Catherine ; Xenophontos, Anastasia ; Clasen, Liv ; Sauls, Bethany ; Seidlitz, Jakob ; Blumenthal, Jonathan ; Torres, Erin ; Thurm, Audrey ; Raznahan, Armin

Journal of neurodevelopmental disorders, 2018-10, Vol.10 (1), p.30-30, Article 30 [Periódico revisado por pares]

England: BioMed Central Ltd

Texto completo disponível

Citações Citado por
9
Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities
Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities

Srinivasan, R. ; Wolstencroft, J. ; Erwood, M. ; Raymond, F. L. ; Bree, M. ; Hall, J. ; Skuse, D.

Journal of intellectual disability research, 2019-05, Vol.63 (5), p.477-488 [Periódico revisado por pares]

England: Wiley Subscription Services, Inc

Texto completo disponível

Citações Citado por
10
Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child
Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child
Material Type:
Artigo 		Adicionar ao Meu Espaço

Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child

Riggan, Kirsten A. ; Close, Sharron ; Allyse, Megan A.

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.404-413

Hoboken, USA: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
Resultados 1 2 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Revistas revisadas por pares (12)

Data de Publicação 

De até
Refinar
  1. Antes de2013  (2)
  2. 2013Até2014  (2)
  3. 2015Até2017  (4)
  4. 2018Até2020  (5)
  5. Após 2020  (3)
  6. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.