Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and CACNA1H[original query] |
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CACNA1H mutations in autism spectrum disorders. The Journal of biological chemistry 2006 Aug 281 (31): 22085-91. Splawski Igor, Yoo Dana S, Stotz Stephanie C, Cherry Allison, Clapham David E, Keating Mark |
A common haplotype containing functional CACNA1H variants is frequently coinherited with increased TPSAB1 copy number. Genetics in medicine : official journal of the American College of Medical Genetics 2017 9 20 (5): 503-512. Lyons Jonathan J, Stotz Stephanie C, Chovanec Jack, Liu Yihui, Lewis Katie L, Nelson Celeste, DiMaggio Thomas, Jones Nina, Stone Kelly D, Sung Heejong, Biesecker Leslie G, Colicos Michael A, Milner Joshua |
Copy number variation in fetal alcohol spectrum disorder. Biochemistry and cell biology = Biochimie et biologie cellulaire 2018 Mar 1-6. Zarrei Mehdi, Hicks Geoffrey G, Reynolds James N, Thiruvahindrapuram Bhooma, Engchuan Worrawat, Pind Molly, Lamoureux Sylvia, Wei John, Wang Zhouzhi, Marshall Christian R, Wintle Richard F, Chudley Albert E, Scherer Stephen |
The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children. Frontiers in neurology 2019 10 505. Long Shasha, Zhou Hao, Li Shuang, Wang Tianqi, Ma Yu, Li Chunpei, Zhou Yuanfeng, Zhou Shuizhen, Wu Bingbing, Wang |
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