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	Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment [My Copy] Genes, Brain & Behavior, Vol. 7, No. 4. (June 2008), pp. 393-402. by Falcaro, , Pickles, et al., Newbury, , Addis, , Banfield, , Fisher, , Monaco, , Simkin, , Conti-Ramsden, posted to genetica sintaxis by islasli on 2009-03-27 13:28:46 as along with 1 person Eugene
	Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. [My Copy] American journal of human genetics, Vol. 71, No. 4. (October 2002), pp. 959-963. by S. L. Smalley, V. Kustanovich, S. L. Minassian, et al.J. L. Stone, M. N. Ogdie, J. J. McGough, J. T. McCracken, I. L. MacPhie, C. Francks, S. E. Fisher, R. M. Cantor, A. P. Monaco, S. F. Nelson posted to genetica by islasli on 2009-03-20 16:11:55 as
	A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. [My Copy] American journal of human genetics, Vol. 70, No. 5. (May 2002), pp. 1183-1196. by S. E. Fisher, C. Francks, J. T. McCracken, et al.J. J. McGough, A. J. Marlow, I. L. MacPhie, D. F. Newbury, L. R. Crawford, C. G. Palmer, J. A. Woodward, M. Del'Homme, D. P. Cantwell, S. F. Nelson, A. P. Monaco, S. L. Smalley posted to genetica by islasli on 2009-03-13 13:25:32 as
	A Genome-Wide Scan of 1842 DNA Markers for Allelic Associations with General Cognitive Ability: A Five-Stage Design Using DNA Pooling and Extreme Selected Groups [My Copy] Behavior Genetics, Vol. 31, No. 6. (1 November 2001), pp. 497-509. by Robert Plomin, Linzy Hill, Ian Craig, et al.Peter Mcguffin, Shaun Purcell, Pak Sham, David Lubinski, Lee Thompson, Paul Fisher, Dragana Turic, Michael Owen posted to genetica by islasli on 2009-01-23 14:58:49 as
	Localisation of a gene implicated in a severe speech and language disorder [My Copy] Nat Genet, Vol. 18, No. 2. (February 1998), pp. 168-170. by Simon E. Fisher, Faraneh Vargha-Khadem, Kate E. Watkins, Anthony P. Monaco, Marcus E. Pembrey posted to genetica lenguaje by islasli on 2009-01-22 18:23:31 as
	A forkhead-domain gene is mutated in a severe speech and language disorder. [My Copy] Nature, Vol. 413, No. 6855. (4 October 2001), pp. 519-523. by C. S. Lai, S. E. Fisher, J. A. Hurst, F. Vargha-Khadem, A. P. Monaco posted to genetica lenguaje by islasli on 2009-01-22 14:23:04 as along with 1 person daforerog
	Molecular evolution of FOXP2, a gene involved in speech and language. [My Copy] Nature, Vol. 418, No. 6900. (22 August 2002), pp. 869-872. by Wolfgang Enard, Molly Przeworski, Simon E. Fisher, et al.Cecilia S. Lai, Victor Wiebe, Takashi Kitano, Anthony P. Monaco, Svante Pääbo posted to genetica lenguaje by islasli on 2009-01-19 00:09:23 as along with 5 people and 1 group jeremymiller cacalaudi niallhaslam djkt rvosa FAB-lab
	FOXP2 in focus: what can genes tell us about speech and language? [My Copy] Trends in Cognitive Sciences, Vol. 7, No. 6. (June 2003), pp. 257-262. by Gary F. Marcus, Simon E. Fisher posted to genetica by islasli on 2009-01-18 23:04:12 as along with 4 people and 1 group cacalaudi garyfeng crispinb margrit ReadingLab
	The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. [My Copy] American journal of human genetics, Vol. 67, No. 2. (August 2000), pp. 357-368. by C. S. Lai, S. E. Fisher, J. A. Hurst, et al.E. R. Levy, S. Hodgson, M. Fox, S. Jeremiah, S. Povey, D. C. Jamison, E. D. Green, F. Vargha-Khadem, A. P. Monaco posted to genetica by islasli on 2009-01-18 18:12:56 as
	FOXP2 is not a major susceptibility gene for autism or specific language impairment. [My Copy] American journal of human genetics, Vol. 70, No. 5. (May 2002), pp. 1318-1327. by D. F. Newbury, E. Bonora, J. A. Lamb, et al.S. E. Fisher, C. S. Lai, G. Baird, L. Jannoun, V. Slonims, C. M. Stott, M. J. Merricks, P. F. Bolton, A. J. Bailey, A. P. Monaco, posted to genetica by islasli on 2009-01-18 00:26:56 as
	DECIPHERING THE GENETIC BASIS OF SPEECH AND LANGUAGE DISORDERS [My Copy] Annual Review of Neuroscience, Vol. 26, No. 1. (2003), pp. 57-80. by Simon E. Fisher, Cecilia S. L. Lai, Anthony P. Monaco posted to genetica by islasli on 2009-01-17 23:02:06 as
	Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. [My Copy] American journal of human genetics, Vol. 76, No. 6. (June 2005), pp. 1074-1080. by Kay D. MacDermot, Elena Bonora, Nuala Sykes, et al.Anne-Marie M. Coupe, Cecilia S. Lai, Sonja C. Vernes, Faraneh Vargha-Khadem, Fiona McKenzie, Robert L. Smith, Anthony P. Monaco, Simon E. Fisher posted to no-tag by islasli on 2009-01-17 22:06:09 as
	A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. [My Copy] American journal of human genetics, Vol. 75, No. 6. (December 2004), pp. 1046-1058. by C. Francks, S. Paracchini, S. D. Smith, et al.A. J. Richardson, T. S. Scerri, L. R. Cardon, A. J. Marlow, I. L. MacPhie, J. Walter, B. F. Pennington, S. E. Fisher, R. K. Olson, J. C. DeFries, J. F. Stein, A. P. Monaco posted to genetica by islasli on 2009-01-16 17:59:48 as

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