Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: RANBP1[original query] |
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Association of RANBP1 haplotype with smooth pursuit eye movement abnormality. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011 Jan 156B (1): 67-71. Cheong Hyun Sub, Park Byung Lae, Kim Eun Mi, Park Chul Soo, Sohn Jin-Wook, Kim Bong-Jo, Kim Jae Won, Kim Ki-Hoon, Shin Tae-Min, Choi Ihn-Geun, Han Sang-Woo, Hwang Jaeuk, Koh InSong, Shin Hyoung Doo, Woo Sung- |
The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder. Scientific reports 2016 6 19372. Wenger Tara L, Kao Charlly, McDonald-McGinn Donna M, Zackai Elaine H, Bailey Alice, Schultz Robert T, Morrow Bernice E, Emanuel Beverly S, Hakonarson Hak |
Variants in LRRC34 reveal distinct mechanisms for predisposition to papillary thyroid carcinoma. Journal of medical genetics 2020 Feb . Comiskey Daniel Forrest, He Huiling, Liyanarachchi Sandya, Sheikh Mehek S, Genutis Luke K, Hendrickson Isabella V, Yu Lianbo, Brock Pamela L, de la Chapelle Albe |
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- Page last updated:Apr 22, 2024
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