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Early symptoms of autism spectrum disorder (ASD) in 1–8 year old children with sex chromosome trisomies (XXX, XXY, XYY), and the predictive value of joint attentionBouw, Nienke ; Swaab, Hanna ; Tartaglia, Nicole ; Wilson, Rebecca L. ; Van der velde, Kim ; van Rijn, SophieEuropean child & adolescent psychiatry, 2023-11, Vol.32 (11), p.2323-2334 [Periódico revisado por pares]Berlin/Heidelberg: Springer Berlin HeidelbergTexto completo disponível |
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XXX SEFC CONGRESSBasic & clinical pharmacology & toxicology, 2018-09, Vol.123 (S4), p.5-6 [Periódico revisado por pares]Oxford: Wiley Subscription Services, IncTexto completo disponível |
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A case‐control study of brain structure and behavioral characteristics in 47,XXX syndromeLenroot, R. K. ; Blumenthal, J. D. ; Wallace, G. L. ; Clasen, L. S. ; Lee, N. R. ; Giedd, J. N.Genes, brain and behavior, 2014-11, Vol.13 (8), p.841-849 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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Early Social Behavior in Young Children with Sex Chromosome Trisomies (XXX, XXY, XYY): Profiles of Observed Social Interactions and Social Impairments Associated with Autism Spectrum Disorder (ASD)Bouw, Nienke ; Swaab, Hanna ; Tartaglia, Nicole ; Cordeiro, Lisa ; van Rijn, SophieJournal of autism and developmental disorders, 2023-08, Vol.53 (8), p.3194-3207 [Periódico revisado por pares]New York: Springer USTexto completo disponível |
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Expression of VEGF b, the inhibitory isoforms of VEGF, in malignant melanomaPritchard-Jones, R O ; Dunn, D B A ; Qiu, Y ; Varey, A H R ; Orlando, A ; Rigby, H ; Harper, S J ; Bates, D OBritish journal of cancer, 2007-07, Vol.97 (2), p.223-230 [Periódico revisado por pares]EnglandTexto completo disponível |
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Patients with 47, XXX karyotype who experienced premature ovarian failure (POF): two case reportsSugawara, Nobuo ; Maeda, Machiko ; Manome, Tomomi ; Nagai, Rie ; Araki, YasuhisaReproductive medicine and biology, 2013-10, Vol.12 (4), p.193-195 [Periódico revisado por pares]Tokyo: Springer JapanTexto completo disponível |
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Author Correction: Double trisomy (XXX+21 karyotype) in a six-year-old girl with down phenotypeVergara-Mendez, Laura Daniela ; Talero-Gutiérrez, Claudia ; Velez-Van-Meerbeke, AlbertoJournal of genetics, 2018-06, Vol.97 (2), p.585-585 [Periódico revisado por pares]New Delhi: Springer IndiaTexto completo disponível |
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Double trisomy (XXX+21 karyotype) in a six-year-old girl with down phenotypeVergara-Mendez, Laura Daniela ; Talero-Gutiérrez, Claudia ; Velez-Van-Meerbeke, AlbertoJournal of genetics, 2018-03, Vol.97 (1), p.337-340 [Periódico revisado por pares]New Delhi: Springer IndiaTexto completo disponível |
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Experiences of mental health services by people with intellectual disabilities from different ethnic groups: a Delphi consultation: Mental Health and Intellectual Disability: XXXBONELL, S ; UNDERWOOD, L ; RADHAKRISHNAN, V ; MCCARTHY, JJournal of intellectual disability research, 2012, Vol.56, p.902-909 [Periódico revisado por pares]Oxford: Wiley-BlackwellTexto completo disponível |
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Structural and numerical changes of chromosome X in patients with esophageal atresiaBrosens, Erwin ; de Jong, Elisabeth M ; Barakat, Tahsin Stefan ; Eussen, Bert H ; D'haene, Barbara ; De Baere, Elfride ; Verdin, Hannah ; Poddighe, Pino J ; Galjaard, Robert-Jan ; Gribnau, Joost ; Brooks, Alice S ; Tibboel, Dick ; de Klein, Annelies2014Sem texto completo |