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Material Type: Artigo
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THE PERSISTENCY IN EXPERIMENTAL POPULATIONS OF SECOND CHROMOSOME RECESSIVE LETHALS OBTAINED AFTER IRRADIATION OF SPERMATOGONIA AND SPERMATOZOA IN DROSOPHILA MELANOGASTERYTTERBORN, KARL H.Hereditas, 1968-01, Vol.60 (1-2), p.33-71 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Chromosomal Abnormalities in Patients With Autism Spectrum Disorders From TaiwanLiao, 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-HsiangAmerican journal of medical genetics. Part B, Neuropsychiatric genetics, 2013-10, Vol.162B (7), p.734-741 [Periódico revisado por pares]United States: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Bornyl caffeate induces apoptosis in human breast cancer MCF-7 cells via the ROS- and JNK-mediated pathwaysYang, Chuan-bin ; Pei, Wei-jing ; Zhao, Jia ; Cheng, Yuan-yuan ; Zheng, Xiao-hui ; Rong, Jian-huiActa pharmacologica Sinica, 2014-01, Vol.35 (1), p.113-123 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Social cognition and underlying cognitive mechanisms in children with an extra X chromosome: a comparison with autism spectrum disordervan 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 LtdTexto completo disponível |
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Material Type: Artigo
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Annual Research Review: Rare genotypes and childhood psychopathology - uncovering diverse developmental mechanisms of ADHD riskScerif, Gaia ; Baker, KateJournal of child psychology and psychiatry, 2015-03, Vol.56 (3), p.251-273 [Periódico revisado por pares]England: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXXSamango-Sprouse, Carole ; Keen, Colleen ; Mitchell, Francie ; Sadeghin, Teresa ; Gropman, AndreaAmerican journal of medical genetics. Part A, 2015-10, Vol.167A (10), p.2251-2259 [Periódico revisado por pares]United States: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosisWigby, Kristen ; D'Epagnier, Cheryl ; Howell, Susan ; Reicks, Amy ; Wilson, Rebecca ; Cordeiro, Lisa ; Tartaglia, NicoleAmerican journal of medical genetics. Part A, 2016-11, Vol.170A (11), p.2870-2881 [Periódico revisado por pares]United States: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Vocal and gestural productions of 24‐month‐old children with sex chromosome trisomiesZampini, Laura ; Draghi, Lara ; Silibello, Gaia ; Dall'Ara, Francesca ; Rigamonti, Claudia ; Suttora, Chiara ; Zanchi, Paola ; Salerni, Nicoletta ; Lalatta, Faustina ; Vizziello, PaolaInternational journal of language & communication disorders, 2018-01, Vol.53 (1), p.171-181 [Periódico revisado por pares]United States: Wiley-BlackwellTexto completo disponível |
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Material Type: Artigo
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Exploring the rationale for combining ionizing radiation and immune checkpoint blockade in head and neck cancerMorisada, Megan ; Chamberlin, Michael ; Allen, ClintHead & neck, 2018-06, Vol.40 (6), p.1321-1334 [Periódico revisado por pares]United States: Wiley Subscription Services, IncTexto completo disponível |
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Material Type: Artigo
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Combining Wolbachia-induced sterility and virus protection to fight Aedes albopictus-borne virusesMoretti, Riccardo ; Yen, Pei-Shi ; Houé, Vincent ; Lampazzi, Elena ; Desiderio, Angiola ; Failloux, Anna-Bella ; Calvitti, Maurizio Simmons, Cameron P.PLoS neglected tropical diseases, 2018-07, Vol.12 (7), p.e0006626-e0006626 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |