-
1
-
-
63449102727
-
FOXP2 as a molecular window into speech and language
-
Fisher SE, Scharff C. FOXP2 as a molecular window into speech and language. Trends Genet 2009;25:166-77.
-
(2009)
Trends Genet
, vol.25
, pp. 166-177
-
-
Fisher, S.E.1
Scharff, C.2
-
2
-
-
57149090343
-
A functional genetic link between distinct developmental language disorders
-
Vernes SC, Newbury DF, Abrahams BS, et al. A functional genetic link between distinct developmental language disorders. N Engl J Med 2008;359:2337-45.
-
(2008)
N Engl J Med
, vol.359
, pp. 2337-2345
-
-
Vernes, S.C.1
Newbury, D.F.2
Abrahams, B.S.3
-
3
-
-
68249126179
-
CMIP and ATP2C2 modulate phonological short-term memory in language impairment
-
Newbury DF, Winchester L, Addis L, et al. CMIP and ATP2C2 modulate phonological short-term memory in language impairment. Am J Hum Genet 2009;85:264-72.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 264-272
-
-
Newbury, D.F.1
Winchester, L.2
Addis, L.3
-
4
-
-
33744925717
-
Genes, cognition and dyslexia: Learning to read the genome
-
Fisher SE, Francks C. Genes, cognition and dyslexia: learning to read the genome. Trends Cogn Sci 2006;10:250-7.
-
(2006)
Trends Cogn Sci
, vol.10
, pp. 250-257
-
-
Fisher, S.E.1
Francks, C.2
-
5
-
-
77349117333
-
Mutations in the lysosomal enzyme -targeting pathway and persistent stuttering
-
Kang C, Riazuddin S, Mundorff J, et al. Mutations in the lysosomal enzyme -targeting pathway and persistent stuttering. N Engl J Med 2010;362:677-85.
-
(2010)
N Engl J Med
, Issue.362
, pp. 677-685
-
-
Kang, C.1
Riazuddin, S.2
Mundorff, J.3
-
6
-
-
0032825726
-
Early childhood stuttering. I. Persistency and recovery rates
-
Yairi E, Ambrose NG. Early childhood stuttering. I. Persistency and recovery rates. J Speech Lang Hear Res 1999;42:1097-112.
-
(1999)
J Speech Lang Hear Res
, vol.42
, pp. 1097-1112
-
-
Yairi, E.1
Ambrose, N.G.2
-
7
-
-
34249738521
-
Genetic etiology in cases of recovered and persistent stuttering in an unselected, longitudinal sample of young twins
-
Dworzynski K, Remington A, Rijsdijk F, Howell P, Plomin R. Genetic etiology in cases of recovered and persistent stuttering in an unselected, longitudinal sample of young twins. Am J Speech Lang Pathol 2007;16:169-78.
-
(2007)
Am J Speech Lang Pathol
, vol.16
, pp. 169-178
-
-
Dworzynski, K.1
Remington, A.2
Rijsdijk, F.3
Howell, P.4
Plomin, R.5
-
8
-
-
15944384953
-
Genomewide significant linkage to stuttering on chromosome 12
-
Riaz N, Steinberg S, Ahmad J, et al. Genomewide significant linkage to stuttering on chromosome 12. Am J Hum Genet 2005; 76:647-51.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 647-651
-
-
Riaz, N.1
Steinberg, S.2
Ahmad, J.3
-
9
-
-
0347417907
-
Results of a genome-wide linkage scan for stuttering
-
Shugart YY, Mundorff J, Kilshaw J, et al. Results of a genome-wide linkage scan for stuttering. Am J Med Genet A 2004; 124A:133-5.
-
(2004)
Am J Med Genet A
, vol.124 A
, pp. 133-135
-
-
Shugart, Y.Y.1
Mundorff, J.2
Kilshaw, J.3
-
10
-
-
33645461964
-
New complexities in the genetics of stuttering: Significant sex-specific linkage signals
-
Suresh R, Ambrose N, Roe C, et al. New complexities in the genetics of stuttering: significant sex-specific linkage signals. Am J Hum Genet 2006;78:554-63.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 554-563
-
-
Suresh, R.1
Ambrose, N.2
Roe, C.3
-
12
-
-
33344471661
-
Mucolipidosis II (I-cell disease) and mucolipidosis IIIA (classical pseudo-Hurler polydystrophy) are caused by mutations in the GlcNAc-phosphotransferase alpha/beta-subunits precursor gene
-
Kudo M, Brem MS, Canfield WM. Mucolipidosis II (I-cell disease) and mucolipidosis IIIA (classical pseudo-Hurler polydystrophy) are caused by mutations in the GlcNAc-phosphotransferase alpha/beta-subunits precursor gene. Am J Hum Genet 2006;78:451-63.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 451-463
-
-
Kudo, M.1
Brem, M.S.2
Canfield, W.M.3
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