Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Epilepsy and MYH11[original query] |
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Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders. PloS one 2013 8 (4): e61365. Tropeano Maria, Ahn Joo Wook, Dobson Richard J B, Breen Gerome, Rucker James, Dixit Abhishek, Pal Deb K, McGuffin Peter, Farmer Anne, White Peter S, Andrieux Joris, Vassos Evangelos, Ogilvie Caroline Mackie, Curran Sarah, Collier David |
Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2019 4 32 (9): 1281-1290. Hata Yukiko, Hirono Keiichi, Yamaguchi Yoshiaki, Ichida Fukiko, Oku Yuko, Nishida Nao |
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- Page last updated:Apr 22, 2024
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