-
1
-
-
0028030006
-
Quantative trait locus for reading disability on chromosome 6
-
Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, De Fries JC (1994) Quantative trait locus for reading disability on chromosome 6. Science 266:276-279
-
(1994)
Science
, vol.266
, pp. 276-279
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
Kimberling, W.J.4
Pennington, B.F.5
De Fries, J.C.6
-
2
-
-
0033366739
-
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
-
Fisher SE, Marlow AJ, Lamb J, Maestrini E, Williams DF, Richardson AJ, Weeks DE, Stein JF, Monaco AP (1999) A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. Am J Hum Genet 64:146-156
-
(1999)
Am J Hum Genet
, vol.64
, pp. 146-156
-
-
Fisher, S.E.1
Marlow, A.J.2
Lamb, J.3
Maestrini, E.4
Williams, D.F.5
Richardson, A.J.6
Weeks, D.E.7
Stein, J.F.8
Monaco, A.P.9
-
3
-
-
0033364213
-
Quantitative-trait locus for specific language and reading deficits on chromosome 6p
-
Gayan J, Smith SD, Cherny SS, Cardon LR, Fulker DW, Brower AM, Olson RK, Pennington BF, De Fries JC (1999) Quantitative-trait locus for specific language and reading deficits on chromosome 6p. Am J Hum Genet 64: 157-164
-
(1999)
Am J Hum Genet
, vol.64
, pp. 157-164
-
-
Gayan, J.1
Smith, S.D.2
Cherny, S.S.3
Cardon, L.R.4
Fulker, D.W.5
Brower, A.M.6
Olson, R.K.7
Pennington, B.F.8
De Fries, J.C.9
-
4
-
-
0031027824
-
Susceptibility loci for distinct components of developmental dyslexia on chromosome 6 and 15
-
Grigorenko EL, Wood FB, Meyer MS, Hart LA, Speed WC, Shuster A, Pauls DL (1997) Susceptibility loci for distinct components of developmental dyslexia on chromosome 6 and 15. Am J Hum Genet 60:27-39
-
(1997)
Am J Hum Genet
, vol.60
, pp. 27-39
-
-
Grigorenko, E.L.1
Wood, F.B.2
Meyer, M.S.3
Hart, L.A.4
Speed, W.C.5
Shuster, A.6
Pauls, D.L.7
-
5
-
-
76549233000
-
Specific dyslexia ('congenital word-blindness'): A clinical and genetic study
-
Hallgren B (1950) Specific dyslexia ('congenital word-blindness'): a clinical and genetic study. Acta Psychiat Neurol Scand 65 (suppl.): 1-287
-
(1950)
Acta Psychiat Neurol Scand
, vol.65
, Issue.SUPPL.
, pp. 1-287
-
-
Hallgren, B.1
-
7
-
-
0002877401
-
Dyslexia subtypes: Genetics, behavior, and brain imaging
-
Duane DD, Gray DB. Parkton, Maryland
-
Lubs HA, Duara R, Levin B, Jallad B, Lubs ML, Rabin M, Kushch A, Gross-Glenn K (1991) Dyslexia subtypes: genetics, behavior, and brain imaging. In: Duane DD, Gray DB: The Reading Brain 89-18. Parkton, Maryland
-
(1991)
The Reading Brain
, pp. 89-118
-
-
Lubs, H.A.1
Duara, R.2
Levin, B.3
Jallad, B.4
Lubs, M.L.5
Rabin, M.6
Kushch, A.7
Gross-Glenn, K.8
-
8
-
-
0039513062
-
Computer-simulation methods in human linkage analysis
-
Ott J (1989) Computer-simulation methods in human linkage analysis. Proc Natl Acad Sci USA 86:4175-4178
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 4175-4178
-
-
Ott, J.1
-
10
-
-
0025992157
-
Evidence for a major gene transmission of developmental dyslexia
-
Pennington BF, Gilger JW, Pauls D, Smith SA, Smith SD, De Fries JC (1991) Evidence for a major gene transmission of developmental dyslexia. JAMA 18:1527-1534
-
(1991)
JAMA
, vol.18
, pp. 1527-1534
-
-
Pennington, B.F.1
Gilger, J.W.2
Pauls, D.3
Smith, S.A.4
Smith, S.D.5
De Fries, J.C.6
-
11
-
-
0032231443
-
Evidence for linkage of spelling disability to chromosome 15
-
Schulte-Körne G, Grimm T, Nöthen M, Müller-Myhsok B, Cichon S, Vogt J, Propping P, Remschmidt H (1998) Evidence for linkage of spelling disability to chromosome 15. Am J Hum Genet 63:279-282
-
(1998)
Am J Hum Genet
, vol.63
, pp. 279-282
-
-
Schulte-Körne, G.1
Grimm, T.2
Nöthen, M.3
Müller-Myhsok, B.4
Cichon, S.5
Vogt, J.6
Propping, P.7
Remschmidt, H.8
-
14
-
-
0001328240
-
Six cases of congenital word-blindness affecting three generations of one family
-
Stephenson S (1907) Six cases of congenital word-blindness affecting three generations of one family. Opthalmoscope 5:482-484
-
(1907)
Opthalmoscope
, vol.5
, pp. 482-484
-
-
Stephenson, S.1
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