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Public Health Reports (Washington, D.C. : 1974)|January 24, 2007
The National Down Syndrome Project: design and implementationSallie B Freeman, Emily G Allen, Cindy L Oxford-Wright, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|October 15, 2013
Identification of the SPLUNC1 ENaC-inhibitory domain yields novel strategies to treat sodium hyperabsorption in cystic fibrosis airway epithelial culturesCarey A Hobbs, Maxime G Blanchard, Omar Alijevic, et al.
Birth Defects Research|October 13, 2022
Differential newborn DNA methylation among individuals with complex congenital heart defects and childhood lymphomaMelissa A Richard, Wei Yang, Pagna Sok, et al.
Ecology and Evolution|December 7, 2018
Ice ages and butterflyfishes: Phylogenomics elucidates the ecological and evolutionary history of reef fishes in an endemism hotspotJoseph D DiBattista, Michael E Alfaro, Laurie Sorenson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2008
Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome ProjectSallie B Freeman, Lora H Bean, Emily G Allen, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 18, 2013
Molecular basis for pH-dependent mucosal dehydration in cystic fibrosis airwaysAlaina L Garland, William G Walton, Raymond D Coakley, et al.
Disability and Rehabilitation. Assistive Technology|June 7, 2018
Assistive technology products: a position paper from the first global research, innovation, and education on assistive technology (GREAT) summitRoger O Smith, Marcia J Scherer, Rory Cooper, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 31, 2008
Next generation of adeno-associated virus 2 vectors: point mutations in tyrosines lead to high-efficiency transduction at lower dosesLi Zhong, Baozheng Li, Cathryn S Mah, et al.
American Journal of Medical Genetics. Part A|August 19, 2023
Novel association of Dandy-Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndromeM Makenzie Beaman, Lucia Guidugli, Monia Hammer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2013
The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome ProjectJessica Ezzell Hunter, Emily Graves Allen, Mikyong Shin, et al.
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