Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: RAB11FIP5[original query] |
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Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population. Molecular autism 2014 5 (1): 5. Matsunami Nori, Hensel Charles H, Baird Lisa, Stevens Jeff, Otterud Brith, Leppert Tami, Varvil Tena, Hadley Dexter, Glessner Joseph T, Pellegrino Renata, Kim Cecilia, Thomas Kelly, Wang Fengxiang, Otieno Frederick G, Ho Karen, Christensen Gerald B, Li Dongying, Prekeris Rytis, Lambert Christophe G, Hakonarson Hakon, Leppert Mark |
Multidimensional Bone Density Phenotyping Reveals New Insights Into Genetic Regulation of the Pediatric Skeleton.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2018 05 33 (5): 812-821. Mitchell Jonathan A, Chesi Alessandra, Cousminer Diana L, McCormack Shana E, Kalkwarf Heidi J, Lappe Joan M, Gilsanz Vicente, Oberfield Sharon E, Shepherd John A, Kelly Andrea, Zemel Babette S, Grant Struan |
Recurrent, low-frequency coding variants contributing to colorectal cancer in the Swedish population. PloS one 2018 13 (3): e0193547. Jiao Xiang, Liu Wen, Mahdessian Hovsep, Bryant Patrick, Ringdahl Jenny, Timofeeva Maria, Farrington Susan M, Dunlop Malcolm, Lindblom Anni |
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- Page last updated:Apr 16, 2024
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