Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Language Disorders 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 |
| Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. European journal of human genetics : EJHG 2009 Oct 17 (10): 1354-8. Vernes Sonja C, MacDermot Kay D, Monaco Anthony P, Fisher Simon |
| Association between FOXP2 gene and speech sound disorder in Chinese population. Psychiatry and clinical neurosciences 2010 Oct 64 (5): 565-73. Zhao Yunjing, Ma Hongwei, Wang Yueping, Gao Hong, Xi Chunyan, Hua Tainyi, Zhao Yaru, Qiu Guangro |
| Assessing the effects of common variation in the FOXP2 gene on human brain structure. Frontiers in human neuroscience 2014 8 473. Hoogman Martine, Guadalupe Tulio, Zwiers Marcel P, Klarenbeek Patricia, Francks Clyde, Fisher Simon |
| FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. Journal of medical genetics 2016 Aug . Reuter Miriam S, Riess Angelika, Moog Ute, Briggs Tracy A, Chandler Kate E, Rauch Anita, Stampfer Miriam, Steindl Katharina, Gläser Dieter, Joset Pascal, , Krumbiegel Mandy, Rabe Harald, Schulte-Mattler Uta, Bauer Peter, Beck-Wödl Stefanie, Kohlhase Jürgen, Reis André, Zweier Christia |
| Genetic variability of FOXP2 and its targets CNTNAP2 and PRNP in frontotemporal dementia: A pilot study in a southern Italian population. Heliyon 2024 6 10 (11): e31624. Paolina Crocco, Francesco De Rango, Francesco Bruno, Antonio Malvaso, Raffaele Maletta, Amalia C Bruni, Giuseppe Passarino, Giuseppina Rose, Serena Da |
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