Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Material Type: Artigo
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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexiaSimpson, Nuala H ; Addis, Laura ; Brandler, William M ; Slonims, Vicky ; Clark, Ann ; Watson, Jocelynne ; Scerri, Thomas S ; Hennessy, Elizabeth R ; Bolton, Patrick F ; Conti‐Ramsden, Gina ; Fairfax, Benjamin P ; Knight, Julian C ; Stein, John ; Talcott, Joel B ; O'Hare, Anne ; Baird, Gillian ; Paracchini, Silvia ; Fisher, Simon E ; Newbury, Dianne F ; Consortium, SLIDevelopmental medicine and child neurology, 2014-04, Vol.56 (4), p.346-353 [Periódico revisado por pares]England: BlackWell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Non-Invasive Prenatal Testing for "Non-Medical" Traits: Ensuring Consistency in Ethical Decision-MakingBowman-Smart, Hilary ; Gyngell, Christopher ; Mand, Cara ; Amor, David J. ; Delatycki, Martin B. ; Savulescu, JulianAmerican journal of bioethics, 2023-03, Vol.23 (3), p.3-20 [Periódico revisado por pares]United States: Taylor & FrancisTexto completo disponível |
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Material Type: Artigo
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A systematic review of the psychological factors associated with returning to sport following injuryArdern, Clare L ; Taylor, Nicholas F ; Feller, Julian A ; Webster, Kate EBritish Journal of Sports Medicine, 2013-11, Vol.47 (17), p.1120-1126 [Periódico revisado por pares]England: BMJ Publishing Group Ltd and British Association of Sport and Exercise MedicineTexto completo disponível |
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Material Type: Artigo
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Ethical issues associated with prenatal screening using non‐invasive prenatal testing for sex chromosome aneuploidyJohnston, Molly ; Warton, Chanelle ; Pertile, Mark D. ; Taylor‐Sands, Michelle ; Delatycki, Martin B. ; Hui, Lisa ; Savulescu, Julian ; Mills, CatherinePrenatal diagnosis, 2023-02, Vol.43 (2), p.226-234 [Periódico revisado por pares]England: Wiley Subscription Services, IncTexto completo disponível |
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Material Type: Artigo
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Comparing generativist and constructivist accounts of the use of the past tense form in early child JapaneseTATSUMI, TOMOKO ; PINE, JULIAN M.Journal of child language, 2016-11, Vol.43 (6), p.1365-1384 [Periódico revisado por pares]Cambridge, UK: Cambridge University PressTexto completo disponível |
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Material Type: Artigo
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Biallelic truncating variants in MAPKAPK5 cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactylyHorn, Denise ; Fernández-Núñez, Elisa ; Gomez-Carmona, Ricardo ; Rivera-Barahona, Ana ; Nevado, Julian ; Schwartzmann, Sarina ; Ehmke, Nadja ; Lapunzina, Pablo ; Otaify, Ghada A. ; Temtamy, Samia ; Aglan, Mona ; Boschann, Felix ; Ruiz-Perez, Victor L.Genetics in medicine, 2021-04, Vol.23 (4), p.679-688 [Periódico revisado por pares]United States: Elsevier IncSem texto completo |
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Material Type: Artigo
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Does error-free use of French negation constitute evidence for Very Early Parameter Setting?JOSEPH, KATE L. ; PINE, JULIAN M.Journal of child language, 2002-02, Vol.29 (1), p.71-86 [Periódico revisado por pares]Cambridge, UK: Cambridge University PressTexto completo disponível |
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Material Type: Artigo
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Experts' opinions on the benefit of an incidental prenatal diagnosis of sex chromosomal aneuploidy: a qualitative interview surveyPieters, J. J. P. M. ; Verhaak, C. M. ; Braat, D. D. M. ; van Leeuwen, E. ; Smits, A. P. T.Prenatal diagnosis, 2012-12, Vol.32 (12), p.1151-1157 [Periódico revisado por pares]England: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Risk factors for severe COVID-19 infection in Brazilian childrenHendler, Jordana Vaz ; Miranda do Lago, Patricia ; Müller, Gabriel Cardozo ; Santana, João Carlos ; Piva, Jefferson Pedro ; Daudt, Liane EstevesThe Brazilian journal of infectious diseases, 2021-11, Vol.25 (6), p.101650-101650, Article 101650 [Periódico revisado por pares]Brazil: Elsevier España, S.L.UTexto completo disponível |
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Material Type: Artigo
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Multi‐institutional experience of genetic diagnosis in Ecuador: National registry of chromosome alterations and polymorphismsPaz‐y‐Miño, César ; Yumiceba, Verónica ; Moreta, Germania ; Paredes, Rosario ; Ruiz, Mónica ; Ocampo, Ligia ; Llamos Paneque, Arianne ; Ochoa Pérez, Catalina ; Ruiz‐Cabezas, Juan Carlos ; Álvarez Vidal, Jenny ; Jiménez Torres, Idarmis ; Vargas‐Vera, Ramón ; Cruz, Fernando ; Guapi N, Víctor Hugo ; Montalván, Martha ; Meneses Álvarez, Sara ; Garzón Castro, Maribel ; Lamar Segura, Elizabeth ; Recalde Báez, María Augusta ; Naranjo, María Elena ; Tambaco Jijón, Nina ; Sinche, María ; Licuy, Pedro ; Burgos, Ramiro ; Porras‐Borja, Fabián ; Echeverría‐Garcés, Gabriela ; Pérez‐Villa, Andy ; Armendáriz‐Castillo, Isaac ; García‐Cárdenas, Jennyfer M. ; Guerrero, Santiago ; Guevara‐Ramírez, Patricia ; López‐Cortés, Andrés ; Zambrano, Ana Karina ; Leone, Paola E.Molecular genetics & genomic medicine, 2020-02, Vol.8 (2), p.e1087-n/a [Periódico revisado por pares]United States: John Wiley & Sons, IncTexto completo disponível |