Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and ZDHHC8[original query] |
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Association of ZDHHC8 polymorphisms 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 2010 Sep 153B (6): 1167-72. Shin Hyoung Doo, Park Byung Lae, Bae Joon Seol, Park Tae Joon, Chun Ji Yong, Park Chul Soo, Sohn Jin-Wook, Kim Bong-Jo, Kang Yeo-Hwa, Kim Jae Won, Kim Ki-Hoon, Shin Tae-Min, Woo Sung- |
Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms. European journal of human genetics : EJHG 2012 Oct 20 (10): 1051-7. Shashi Vandana, Francis Alan, Hooper Stephen R, Kranz Peter G, Zapadka Michael, Schoch Kelly, Ip Edward, Tandon Neeraj, Howard Timothy D, Keshavan Matcheri |
Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome. The Journal of biological chemistry 2015 Sep 290 (38): 23240-53. Napoli Eleonora, Tassone Flora, Wong Sarah, Angkustsiri Kathleen, Simon Tony J, Song Gyu, Giulivi Cecil |
Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Jan . Thompson Carlie A, Karelis Jason, Middleton Frank A, Gentile Karen, Coman Ioana L, Radoeva Petya D, Mehta Rashi, Fremont Wanda P, Antshel Kevin M, Faraone Stephen V, Kates Wendy |
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