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2 documents found
1: Title: Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.
Authors: Peter, Beate, et.al. .
Journal: PloS one, Vol. 11 (4): e0153864, 2016 .
Snippet: Single-point linkage analysis of selected variants identified CDH18 as a primary gene of interest and additionally, MYO10, NIPBL, GLP2R, NCOR1, FLCN, SMCR8, NEK8, and ANKRD12, possibly with additive effects.
Affiliation: Dpt. of Speech and Hearing Sciences, Arizona State University, Tempe, Arizona, United States of America. Dpt. of Communication Sciences and Disorders, Saint Louis University, Saint Louis, Missouri, United States of America. Dpt. of Speech and Hearing Sciences, University of Washington, Seattle, Washington, United States of America. Div. of Medical Genetics, Dpt. of Medicine, University of Washington, Seattle, Washington, United States of America. Dpt. of Biostatistics, University of Washington, Seattle, Washington, United States of America. Dpt. of Communication Sciences and Disorders, University of Utah, Salt Lake City, Utah, United States of America. Dpt. of Environmental and Occupational Health, Environmental Toxicology, University of Washington, Seattle, Washington, United States of America. Dpt. of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, United States of America. .
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2: Title: Clinical significance of Ankyrin repeat domain 12 expression in colorectal cancer.
Authors: Bai, Rui, et.al. .
Journal: Journal of experimental & clinical cancer research : CR (J Exp Clin Cancer Res), Vol. 32 (1): 35, 2013 .
Snippet: The ANKRD12 mRNA expression was measured by quantitative real time reverse transcriptase polymerase chain reaction.
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