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Content Provider : Digital Access to Scholarship at Harvard (DASH) Subject : pediatrics فلترة بواسطة : موضوع

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Academic Journal

Perinatal Natural History of the Ts1Cje Mouse Model of Down Syndrome: Growth Restriction, Early Mortality, Heart Defects, and Delayed Development

Authors : Ferrés, Millie A.; Bianchi, Diana W.; Siegel, Ashley E.

Subjects: Model Organisms; Animal Models; Mouse Models

Source: Ferrés, Millie A., Diana W. Bianchi, Ashley E. Siegel, Roderick T. Bronson, Gordon S. Huggins, and Faycal Guedj. 2016. “Perinatal Natural History of the Ts1Cje Mouse Model of Down Syndrome: Growth

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Expectation versus Reality: The Impact of Utility on Emotional Outcomes after Returning Individualized Genetic Research Results in Pediatric Rare Disease Research, a Qualitative Interview Study

Authors : Cacioppo, Cara N.; Chandler, Ariel E.; Towne, Meghan C.

Subjects: Biology and Life Sciences; Psychology; Emotions

Source: Cacioppo, Cara N., Ariel E. Chandler, Meghan C. Towne, Alan H. Beggs, and Ingrid A. Holm. 2016. “Expectation versus Reality: The Impact of Utility on Emotional Outcomes after Returning

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Mapping Genetically Controlled Neural Circuits of Social Behavior and Visuo-Motor Integration by a Preliminary Examination of Atypical Deletions with Williams Syndrome

Authors : Hoeft, Fumiko; Dai, Li; Haas, Brian W.

Subjects: Biology and Life Sciences; Genetics; Genetics of Disease

Source: Hoeft, Fumiko, Li Dai, Brian W. Haas, Kristen Sheau, Masaru Mimura, Debra Mills, Albert Galaburda, Ursula Bellugi, Julie R. Korenberg, and Allan L. Reiss. 2014. “Mapping Genetically Controlled

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Estimation of Newborn Risk for Child or Adolescent Obesity: Lessons from Longitudinal Birth Cohorts

Authors : Morandi, Anita; Meyre, David; Lobbens, Stéphane

Subjects: Medicine; Clinical Genetics; Clinical Research Design

Source: Morandi, Anita, David Meyre, Stéphane Lobbens, Ken Paul Kleinman, Marika Kaakinen, Sheryl Lynn Rifas-Shiman, Vincent Vatin, et al. 2012. Estimation of newborn risk for child or adolescent obesity:

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Loss-of-Function Mutations in PTPN11 Cause Metachondromatosis, But Not Ollier Disease or Maffucci Syndrome

Authors : Campos-Xavier, Belinda; Superti-Furga, Andrea; Ikegawa, Shiro

Subjects: biology; genetics; cancer genetics

Source: Bowen, Margot E., Eric D. Boyden, Ingrid A. Holm, Belinda Campos-Xavier, Luisa Bonafé, Andrea Superti-Furga, Shiro Ikegawa, and et al. 2011. Loss-of-function mutations in PTPN11 cause

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