Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Autistic Disorder and FOXP2[original query] |
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Mutation screening of FOXP2 in individuals diagnosed with autistic disorder. American journal of medical genetics. Part A 2003 Apr 118A (2): 172-5. Gauthier Julie, Joober Ridha, Mottron Laurent, Laurent Sandra, Fuchs Marketa, De Kimpe Violaine, Rouleau Guy |
Association study of the CNS patterning genes and autism in Han Chinese in Taiwan. Progress in neuro-psychopharmacology & biological psychiatry 2011 Aug 35 (6): 1512-7. Chien Yi-Ling, Wu Yu-Yu, Chiu Yen-Nan, Liu Shih-Kai, Tsai Wen-Che, Lin Ping-I, Chen Chia-Hsiang, Gau Susan Shur-Fen, Chien Wei-Hsi |
The WNT2 gene polymorphism associated with speech delay inherent to autism. Research in developmental disabilities 0 33 (5): 1533-40. Lin Ping-I, Chien Yi-Ling, Wu Yu-Yu, Chen Chia-Hsiang, Gau Susan Shur-Fen, Huang Yu-Shu, Liu Shih-Kai, Tsai Wen-Che, Chiu Yen-N |
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