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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 1, 2023. (Total: 221588Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Learning and FOXP2[original query]
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
An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples.
Psychiatric genetics 2012 Aug 22 (4): 155-60.
Ribasés Marta, Sánchez-Mora Cristina, Ramos-Quiroga Josep Antoni, Bosch Rosa, Gómez Núria, Nogueira Mariana, Corrales Montse, Palomar Gloria, Jacob Christian P, Gross-Lesch Silke, Kreiker Susanne, Reif Andreas, Lesch Klaus Peter, Cormand Bru, Casas Miquel, Bayés Móni
Investigation of the forkhead box protein P2 gene by the next-generation sequence analysis method in children diagnosed with specific learning disorder.
Psychiatric genetics 2023 1 33 (1): 8-19.
Yaz?c? Merve, Yekta? Çi?dem, Eröz Recep, Kaplan Karakaya Elif Sümeyra, Sar?gedik En
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