-
1
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis G, Cherny S, Cookson W, Cardon L (2002) Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30:97-101
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.1
Cherny, S.2
Cookson, W.3
Cardon, L.4
-
2
-
-
0000047525
-
Longitudinal follow-up of children with preschool communication disorders: Treatment implications
-
Aram DM, Hall NC (1989) Longitudinal follow-up of children with preschool communication disorders: treatment implications. School Psych Rev 18:487-501
-
(1989)
School Psych Rev
, vol.18
, pp. 487-501
-
-
Aram, D.M.1
Hall, N.C.2
-
3
-
-
0025602128
-
A prospective study of the relationship between specific language impairment, phonological disorders, and reading retardation
-
Bishop D, Adams C (1990) A prospective study of the relationship between specific language impairment, phonological disorders, and reading retardation. J Child Psychol Psychiatry 31:1027-1050
-
(1990)
J Child Psychol Psychiatry
, vol.31
, pp. 1027-1050
-
-
Bishop, D.1
Adams, C.2
-
4
-
-
0029865799
-
Nonword repetition as a behavioural marker for inherited language impairment: Evidence from a twin study
-
Bishop D, North T, Donlan C (1996) Nonword repetition as a behavioural marker for inherited language impairment: evidence from a twin study. J Child Psychol Psychiatry 37: 391-403
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 391-403
-
-
Bishop, D.1
North, T.2
Donlan, C.3
-
5
-
-
0028030006
-
Quantitative trait locus for reading disability on chromosome 6
-
Cardon L, Smith S, Fulker D, Kimberling W, Pennington B, DeFries J (1994) Quantitative trait locus for reading disability on chromosome 6. Science 266:276-279
-
(1994)
Science
, vol.266
, pp. 276-279
-
-
Cardon, L.1
Smith, S.2
Fulker, D.3
Kimberling, W.4
Pennington, B.5
DeFries, J.6
-
6
-
-
0029003528
-
Quantitative trait locus for reading disability: Correction
-
- (1995) Quantitative trait locus for reading disability: correction. Science 268:1553
-
(1995)
Science
, vol.268
, pp. 1553
-
-
-
7
-
-
0022792396
-
Speech production/phonological deficits in reading disordered children
-
Catts H (1986) Speech production/phonological deficits in reading disordered children. J Learn Disabil 19:504-508
-
(1986)
J Learn Disabil
, vol.19
, pp. 504-508
-
-
Catts, H.1
-
8
-
-
0035208755
-
Sample size requirements to control for stochastic variation in magnitude and location of allele-sharing linkage statistics in affected sibling pairs
-
Cordell H (2001) Sample size requirements to control for stochastic variation in magnitude and location of allele-sharing linkage statistics in affected sibling pairs. Ann Hum Genet 65:491-502
-
(2001)
Ann Hum Genet
, vol.65
, pp. 491-502
-
-
Cordell, H.1
-
9
-
-
23044518686
-
History and significance of rapid auditory naming
-
Denckla M, Cutting L (1999) History and significance of rapid auditory naming. Ann Dyslexia 49:29-42
-
(1999)
Ann Dyslexia
, vol.49
, pp. 29-42
-
-
Denckla, M.1
Cutting, L.2
-
10
-
-
0017140877
-
Rapid "automatized" naming (R.A.N.): Dyslexia differentiated from other learning disabilities
-
Denckla M, Rudel R (1976) Rapid "automatized" naming (R.A.N.): dyslexia differentiated from other learning disabilities. Neuropsychologia 14:471-479
-
(1976)
Neuropsychologia
, vol.14
, pp. 471-479
-
-
Denckla, M.1
Rudel, R.2
-
11
-
-
0031472342
-
A variance components approach to dichotomous trait linkage analysis using a threshold model
-
Duggirala R, Williams J, Williams-Blangero S, Blangero J (1997) A variance components approach to dichotomous trait linkage analysis using a threshold model. Genet Epidemiol 14:987-992
-
(1997)
Genet Epidemiol
, vol.14
, pp. 987-992
-
-
Duggirala, R.1
Williams, J.2
Williams-Blangero, S.3
Blangero, J.4
-
13
-
-
0018567215
-
Major locus analysis for quantitative traits
-
Elston R (1979) Major locus analysis for quantitative traits. Am J Hum Genet 31:655-661
-
(1979)
Am J Hum Genet
, vol.31
, pp. 655-661
-
-
Elston, R.1
-
15
-
-
0032877882
-
A new gene (DYX3) for dyslexia is located on chromosome 2
-
Fagerheim T, Raeymaekers P, Tonnessen FE, Pedersen M, Tranebjaerg L, Lubs HA (1999) A new gene (DYX3) for dyslexia is located on chromosome 2. J Med Genet 36:664-669
-
(1999)
J Med Genet
, vol.36
, pp. 664-669
-
-
Fagerheim, T.1
Raeymaekers, P.2
Tonnessen, F.E.3
Pedersen, M.4
Tranebjaerg, L.5
Lubs, H.A.6
-
16
-
-
0028822480
-
Familial aggregation of phonological disorders: Results from a 28 year follow-up
-
Felsenfeld S, McGue M, Broen P (1995) Familial aggregation of phonological disorders: results from a 28 year follow-up. J Speech Hear Res 38:1091-1107
-
(1995)
J Speech Hear Res
, vol.38
, pp. 1091-1107
-
-
Felsenfeld, S.1
McGue, M.2
Broen, P.3
-
17
-
-
0036779497
-
Developmental dyslexia: Genetic dissection of a complex cognitive trait
-
Fisher S, DeFries J (2002) Developmental dyslexia: genetic dissection of a complex cognitive trait. Nat Rev Neurosci 3: 767-780
-
(2002)
Nat Rev Neurosci
, vol.3
, pp. 767-780
-
-
Fisher, S.1
DeFries, J.2
-
18
-
-
18544365699
-
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
-
Fisher S, Francks C, Marlow A, MacPhie I, Newbury D, Cardon L, Ishikawa-Brush Y, Richardson AJ, Talcott JB, Gayan J, Olson RK, Pennington BF, Smith SD, Stein JF, Monaco AP (2002a) Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat Genet 30:86-91
-
(2002)
Nat Genet
, vol.30
, pp. 86-91
-
-
Fisher, S.1
Francks, C.2
Marlow, A.3
MacPhie, I.4
Newbury, D.5
Cardon, L.6
Ishikawa-Brush, Y.7
Richardson, A.J.8
Talcott, J.B.9
Gayan, J.10
Olson, R.K.11
Pennington, B.F.12
Smith, S.D.13
Stein, J.F.14
Monaco, A.P.15
-
19
-
-
0036239098
-
A genomewide scan for loci involved in attention-deficit/hyperactivity disorder
-
Fisher S, Francks C, McCracken J, McGough J, Marlow A, MacPhie I, Newbury D, Crawford LR, Palmer CGS, Woodward JA, Del'Homme M, Cantwell DP, Nelson DP, Monaco AP, Smalley SL (2002b) A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. Am J Hum Genet 70:1183-1196
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1183-1196
-
-
Fisher, S.1
Francks, C.2
McCracken, J.3
McGough, J.4
Marlow, A.5
MacPhie, I.6
Newbury, D.7
Crawford, L.R.8
Palmer, C.G.S.9
Woodward, J.A.10
Del'Homme, M.11
Cantwell, D.P.12
Nelson, D.P.13
Monaco, A.P.14
Smalley, S.L.15
-
20
-
-
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
-
21
-
-
0031940694
-
Localisation of a gene implicated in a severe speech and language disorder
-
Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME (1998) Localisation of a gene implicated in a severe speech and language disorder. Nat Genet 18:168-170
-
(1998)
Nat Genet
, vol.18
, pp. 168-170
-
-
Fisher, S.E.1
Vargha-Khadem, F.2
Watkins, K.E.3
Monaco, A.P.4
Pembrey, M.E.5
-
22
-
-
0036217207
-
Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: Quantitative association analysis and positional candidate genes SEMA4F and OTX1
-
Francks C, Fisher SE, Olson RK, Pennington BF, Smith SD, DeFries JC, Monaco A (2002) Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. Psychiatr Genet 12:35-41
-
(2002)
Psychiatr Genet
, vol.12
, pp. 35-41
-
-
Francks, C.1
Fisher, S.E.2
Olson, R.K.3
Pennington, B.F.4
Smith, S.D.5
DeFries, J.C.6
Monaco, A.7
-
24
-
-
0033364213
-
Quantitative-trait locus for specific language and reading deficits on chromosome 6p
-
Gayan J, Smith S, Cherny S, Cardon L, Fulker D, Brower A, Olson R, Pennington BF, DeFries 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.2
Cherny, S.3
Cardon, L.4
Fulker, D.5
Brower, A.6
Olson, R.7
Pennington, B.F.8
DeFries, J.C.9
-
26
-
-
0042319316
-
Continuing the search for dyslexia genes on 6p
-
Grigorenko E, Wood F, Golovyan L, Meyer M, Romano C, Pauls D (2003) Continuing the search for dyslexia genes on 6p. Am J Med Genet 118B:89-98
-
(2003)
Am J Med Genet
, vol.118 B
, pp. 89-98
-
-
Grigorenko, E.1
Wood, F.2
Golovyan, L.3
Meyer, M.4
Romano, C.5
Pauls, D.6
-
27
-
-
0031027824
-
Susceptibility loci for distinct components of developmental dyslexia on chromosome 6 and 15
-
Grigorenko E, Wood F, Meyer M, Hart L, Speed W, Shuster A, Pauls D (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.1
Wood, F.2
Meyer, M.3
Hart, L.4
Speed, W.5
Shuster, A.6
Pauls, D.7
-
28
-
-
0035825196
-
Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p
-
Grigorenko EL, Wood FB, Meyer MS, Pauls JE, Hart LA, Pauls DL (2001) Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p. Am J Med Genet 105:120-129
-
(2001)
Am J Med Genet
, vol.105
, pp. 120-129
-
-
Grigorenko, E.L.1
Wood, F.B.2
Meyer, M.S.3
Pauls, J.E.4
Hart, L.A.5
Pauls, D.L.6
-
29
-
-
0015309467
-
The investigation of linkage between a quantitative trait and a marker locus
-
Haseman J, Elston R (1972) The investigation of linkage between a quantitative trait and a marker locus. Behav Genet 2:3-19
-
(1972)
Behav Genet
, vol.2
, pp. 3-19
-
-
Haseman, J.1
Elston, R.2
-
31
-
-
0022811868
-
Toward an understanding of developmental language disorders and reading disorders
-
Kamhi A, Catts H (1986) Toward an understanding of developmental language disorders and reading disorders. J Speech Hear Disord 51:337-347
-
(1986)
J Speech Hear Disord
, vol.51
, pp. 337-347
-
-
Kamhi, A.1
Catts, H.2
-
32
-
-
0038577166
-
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32
-
Kaminen N, Hannula-Jouppi K, Kestila M, Lahermo P, Muller K, Kaaranen M, Myllyluoma B, Voutilainen A, Lyytinen H, Nopola-Hemmi J, Kere J (2003) A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32. J Med Genet 40:340-345
-
(2003)
J Med Genet
, vol.40
, pp. 340-345
-
-
Kaminen, N.1
Hannula-Jouppi, K.2
Kestila, M.3
Lahermo, P.4
Muller, K.5
Kaaranen, M.6
Myllyluoma, B.7
Voutilainen, A.8
Lyytinen, H.9
Nopola-Hemmi, J.10
Kere, J.11
-
33
-
-
18344374003
-
Evidence for linkage and association with reading ability on 6p21.3-22
-
Kaplan DE, Gayan J, Ahn J, Won TW, Pauls D, Olson RK, DeFries JC, Wood F, Pennington BF, Page GP, Smith SD, Gruen JR (2002) Evidence for linkage and association with reading ability on 6p21.3-22. Am J Hum Genet 70:1287-1298
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1287-1298
-
-
Kaplan, D.E.1
Gayan, J.2
Ahn, J.3
Won, T.W.4
Pauls, D.5
Olson, R.K.6
DeFries, J.C.7
Wood, F.8
Pennington, B.F.9
Page, G.P.10
Smith, S.D.11
Gruen, J.R.12
-
35
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L (1995) Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 11:241-247
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
36
-
-
0026953733
-
Pedigree analysis of children with phonology disorders
-
Lewis B (1992) Pedigree analysis of children with phonology disorders. J Learn Disabil 25:586-597
-
(1992)
J Learn Disabil
, vol.25
, pp. 586-597
-
-
Lewis, B.1
-
37
-
-
0027300757
-
Segregation analysis of speech and language disorders
-
Lewis B, Cox N, Byard P (1993) Segregation analysis of speech and language disorders. Behav Genet 23:291-297
-
(1993)
Behav Genet
, vol.23
, pp. 291-297
-
-
Lewis, B.1
Cox, N.2
Byard, P.3
-
38
-
-
0024790239
-
A familial study of severe phonological disorders
-
Lewis B, Ekelman B, Aram D (1989) A familial study of severe phonological disorders. J Speech Hear Res 32:713-724
-
(1989)
J Speech Hear Res
, vol.32
, pp. 713-724
-
-
Lewis, B.1
Ekelman, B.2
Aram, D.3
-
39
-
-
0141917779
-
Speech production skills of nuclear family members of children with phonology disorders
-
Lewis B, Freebairn L (1998) Speech production skills of nuclear family members of children with phonology disorders. Lang Speech 41:45-61
-
(1998)
Lang Speech
, vol.41
, pp. 45-61
-
-
Lewis, B.1
Freebairn, L.2
-
40
-
-
0039929221
-
Follow-up of children with early expressive phonology disorders
-
Lewis B, Freebairn L, Taylor H (2000) Follow-up of children with early expressive phonology disorders. J Learn Disabil 33:433-444
-
(2000)
J Learn Disabil
, vol.33
, pp. 433-444
-
-
Lewis, B.1
Freebairn, L.2
Taylor, H.3
-
41
-
-
0026499677
-
A study of developmental speech and language disorders in twins
-
Lewis B, Thompson L (1992) A study of developmental speech and language disorders in twins. J Speech Hear Res 35: 1086-1094
-
(1992)
J Speech Hear Res
, vol.35
, pp. 1086-1094
-
-
Lewis, B.1
Thompson, L.2
-
42
-
-
0037371605
-
Use of multivariate linkage analysis for dissection of a complex trait
-
Marlow A, Fisher S, Francks C, MacPhie I, Cherny S, Richardson A, Talcott J, Stein JF, Monaco AP, Cardon LR (2003) Use of multivariate linkage analysis for dissection of a complex trait. Am J Hum Genet 72:561-570
-
(2003)
Am J Hum Genet
, vol.72
, pp. 561-570
-
-
Marlow, A.1
Fisher, S.2
Francks, C.3
MacPhie, I.4
Cherny, S.5
Richardson, A.6
Talcott, J.7
Stein, J.F.8
Monaco, A.P.9
Cardon, L.R.10
-
43
-
-
0026409530
-
Predicting reading problems in at-risk children
-
Menyuk P, Chesnick M, Liebergott J, Korngold B, D'Agostino R, Belanger A (1991) Predicting reading problems in at-risk children. J Speech Hear Res 34:893-903
-
(1991)
J Speech Hear Res
, vol.34
, pp. 893-903
-
-
Menyuk, P.1
Chesnick, M.2
Liebergott, J.3
Korngold, B.4
D'Agostino, R.5
Belanger, A.6
-
44
-
-
0031031235
-
An examination of word frequency and neighborhood density on development of spoken-word recognition
-
Metsala JL (1997) An examination of word frequency and neighborhood density on development of spoken-word recognition. Mem Cognit 25:47-56
-
(1997)
Mem Cognit
, vol.25
, pp. 47-56
-
-
Metsala, J.L.1
-
46
-
-
0034785618
-
A dominant gene for developmental dyslexia on chromosome 3
-
Nopola-Hemmi J, Myllyluoma B, Haltia T, Taipale M, Ollikainen V, Ahonen T, Voutilainen A, Kere J, Widen E (2001) A dominant gene for developmental dyslexia on chromosome 3. J Med Genet 38:658-664
-
(2001)
J Med Genet
, vol.38
, pp. 658-664
-
-
Nopola-Hemmi, J.1
Myllyluoma, B.2
Haltia, T.3
Taipale, M.4
Ollikainen, V.5
Ahonen, T.6
Voutilainen, A.7
Kere, J.8
Widen, E.9
-
47
-
-
0036727070
-
Familial dyslexia: Neurocognitive and genetic correlation in a large Finnish family
-
Nopola-Hemmi J, Myllyluoma B, Voutilainen A, Leinonen S, Kere J, Ahonen T (2002) Familial dyslexia: neurocognitive and genetic correlation in a large Finnish family. Dev Med Child Neurol 44:580-586
-
(2002)
Dev Med Child Neurol
, vol.44
, pp. 580-586
-
-
Nopola-Hemmi, J.1
Myllyluoma, B.2
Voutilainen, A.3
Leinonen, S.4
Kere, J.5
Ahonen, T.6
-
48
-
-
0344496507
-
Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15
-
Nothen MM, Schulte-Korne G, Grimm T, Chichon S, Vogt IR, Muller-Myhsok B, Propping P, Remschmidt H (1999) Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15. Eur Child Adolesc Psychiatry 8:56-59
-
(1999)
Eur Child Adolesc Psychiatry
, vol.8
, pp. 56-59
-
-
Nothen, M.M.1
Schulte-Korne, G.2
Grimm, T.3
Chichon, S.4
Vogt, I.R.5
Muller-Myhsok, B.6
Propping, P.7
Remschmidt, H.8
-
49
-
-
0035345557
-
Early reading development in children at family risk for dyslexia
-
Pennington B, Lefly D (2001) Early reading development in children at family risk for dyslexia. Child Dev 72:816-833
-
(2001)
Child Dev
, vol.72
, pp. 816-833
-
-
Pennington, B.1
Lefly, D.2
-
50
-
-
0035828096
-
Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia
-
Petryshen TL, Kaplan BJ, Fu Liu M, de French NS, Tobias R, Hughes ML, Field LL (2001) Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia. Am J Med Genet 105:507-517
-
(2001)
Am J Med Genet
, vol.105
, pp. 507-517
-
-
Petryshen, T.L.1
Kaplan, B.J.2
Fu Liu, M.3
De French, N.S.4
Tobias, R.5
Hughes, M.L.6
Field, L.L.7
-
51
-
-
0036168959
-
Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families
-
Petryshen TL, Kaplan BJ, Hughes ML, Tzenova J, Field LL (2002) Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families. J Med Genet 39:125-126
-
(2002)
J Med Genet
, vol.39
, pp. 125-126
-
-
Petryshen, T.L.1
Kaplan, B.J.2
Hughes, M.L.3
Tzenova, J.4
Field, L.L.5
-
52
-
-
0027213075
-
Suggestive linkage of developmental dyslexia to chromosome 1p34-p36
-
Rabin M, Wen XL, Hepburn M, Lubs HA, Feldman E, Duara R (1993) Suggestive linkage of developmental dyslexia to chromosome 1p34-p36. Lancet 342:178
-
(1993)
Lancet
, vol.342
, pp. 178
-
-
Rabin, M.1
Wen, X.L.2
Hepburn, M.3
Lubs, H.A.4
Feldman, E.5
Duara, R.6
-
55
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
Risch N (2000) Searching for genetic determinants in the new millennium. Nature 405:847-856
-
(2000)
Nature
, vol.405
, pp. 847-856
-
-
Risch, N.1
-
56
-
-
0023391805
-
Clinical assessment of oropharyngeal motor development in young children
-
Robbins J, Klee T (1987) Clinical assessment of oropharyngeal motor development in young children. J Speech Hear Disord 52:271-277
-
(1987)
J Speech Hear Disord
, vol.52
, pp. 271-277
-
-
Robbins, J.1
Klee, T.2
-
57
-
-
85047669754
-
Word-frequency and phonological-neighborhood effects on verbal short-term memory
-
Roodenrys S, Hulme C, Lethbridge A, Hinton M, Nimmo LM (2002) Word-frequency and phonological-neighborhood effects on verbal short-term memory. J Exp Psychol Learn Mem Cogn 28:1019-1034
-
(2002)
J Exp Psychol Learn Mem Cogn
, vol.28
, pp. 1019-1034
-
-
Roodenrys, S.1
Hulme, C.2
Lethbridge, A.3
Hinton, M.4
Nimmo, L.M.5
-
58
-
-
85030898240
-
Statistical analysis for genetic epidemiology
-
Cork, Ireland
-
S.A.G.E. (2003) Statistical analysis for genetic epidemiology. Statistical Solutions, Cork, Ireland
-
(2003)
Statistical Solutions
-
-
-
59
-
-
85030902885
-
Broad phenotype of speech disorders shows strong evidence of linkage at candidate region 7q31
-
Paper presented. Strasbourg, France, May 25-28
-
Schick J, Kundtz A, Tiwari H, Taylor H, Freebairn L, Hansen A, Shriberg L, Lewis BA, Iyengar SK (2002) Broad phenotype of speech disorders shows strong evidence of linkage at candidate region 7q31. Paper presented at the European Human Genetics Conference. Strasbourg, France, May 25-28
-
(2002)
European Human Genetics Conference
-
-
Schick, J.1
Kundtz, A.2
Tiwari, H.3
Taylor, H.4
Freebairn, L.5
Hansen, A.6
Shriberg, L.7
Lewis, B.A.8
Iyengar, S.K.9
-
60
-
-
0032231443
-
Evidence for linkage of spelling disability to chromosome 15
-
Schulte-Körne G, Grimm T, Nöthen MM, Müller-Myhsok B, Cichon S, Vogt IR, 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.M.3
Müller-Myhsok, B.4
Cichon, S.5
Vogt, I.R.6
Propping, P.7
Remschmidt, H.8
-
62
-
-
0041884859
-
Adding further power to the Haseman and Elston method for detecting linkage in larger sibships: Weighting sums and differences
-
Shete S, Jacobs K, Elston R (2003) Adding further power to the Haseman and Elston method for detecting linkage in larger sibships: weighting sums and differences. Hum Hered 55:79-85
-
(2003)
Hum Hered
, vol.55
, pp. 79-85
-
-
Shete, S.1
Jacobs, K.2
Elston, R.3
-
63
-
-
0027500636
-
Four new speech and prosody voice measures for genetics research and other studies in developmental phonological disorders
-
Shriberg L (1993) Four new speech and prosody voice measures for genetics research and other studies in developmental phonological disorders. J Speech Hear Res 36:105-140
-
(1993)
J Speech Hear Res
, vol.36
, pp. 105-140
-
-
Shriberg, L.1
-
64
-
-
37349032847
-
Classification and misclassification of child speech sound disorders
-
Paper presented. Atlanta, November 20-24
-
- (2002) Classification and misclassification of child speech sound disorders. Paper presented at the Annual Convention of the American Speech-Language-Hearing Association. Atlanta, November 20-24
-
(2002)
Annual Convention of the American Speech-Language-Hearing Association
-
-
-
65
-
-
0001778409
-
Comorbidity of speech-language disorder: Implications for a phenotype marker for speech delay
-
Paul R (ed). Brookes, Baltimore
-
Shriberg L, Austin D (1998) Comorbidity of speech-language disorder: implications for a phenotype marker for speech delay. In: Paul R (ed) Exploring the speech/language connection. Brookes, Baltimore, pp 73-118
-
(1998)
Exploring the Speech/Language Connection
, pp. 73-118
-
-
Shriberg, L.1
Austin, D.2
-
66
-
-
0030743089
-
The percentage of consonants correct (PCC) metric: Extensions and reliability data
-
Shriberg L, Austin D, Lewis B, McSweeny J, Wilson D (1997) The percentage of consonants correct (PCC) metric: Extensions and reliability data. J Speech Lang Hear Res 40:708-722
-
(1997)
J Speech Lang Hear Res
, vol.40
, pp. 708-722
-
-
Shriberg, L.1
Austin, D.2
Lewis, B.3
McSweeny, J.4
Wilson, D.5
-
68
-
-
0023932746
-
A follow-up of children of phonological disorders of unknown origin
-
Shriberg L, Kwiatkowski J (1988) A follow-up of children of phonological disorders of unknown origin. J Speech Hear Res 53:144-155
-
(1988)
J Speech Hear Res
, vol.53
, pp. 144-155
-
-
Shriberg, L.1
Kwiatkowski, J.2
-
69
-
-
0032761073
-
Prevalence of speech delay in 6-year-old children and comorbidity with language impairment
-
Shriberg L, Tomblin J, McSweeny J (1999) Prevalence of speech delay in 6-year-old children and comorbidity with language impairment. J Speech Lang Hear Res 42:1461-1481
-
(1999)
J Speech Lang Hear Res
, vol.42
, pp. 1461-1481
-
-
Shriberg, L.1
Tomblin, J.2
McSweeny, J.3
-
70
-
-
18244408330
-
A genome-wide scan identifies two novel loci involved in specific language impairment
-
Specific Language Impairment Consortium (2002) A genome-wide scan identifies two novel loci involved in specific language impairment. Am J Hum Genet 70:384-398
-
(2002)
Am J Hum Genet
, vol.70
, pp. 384-398
-
-
-
71
-
-
34248661821
-
Structural equation model-based genome scan for metabolic syndrome
-
Stein CM, Song Y, Elston RC, Jun G, Tiwari HK, Iyengar SK (2003) Structural equation model-based genome scan for metabolic syndrome. BMC Genetics 4 Suppl 1:S99
-
(2003)
BMC Genetics
, vol.4
, Issue.SUPPL. 1
-
-
Stein, C.M.1
Song, Y.2
Elston, R.C.3
Jun, G.4
Tiwari, H.K.5
Iyengar, S.K.6
-
72
-
-
0031890655
-
The heritability of poor language achievement among twins
-
Tomblin J, Buckwalter P (1998) The heritability of poor language achievement among twins. J Speech Lang Hear Res 41:188-199
-
(1998)
J Speech Lang Hear Res
, vol.41
, pp. 188-199
-
-
Tomblin, J.1
Buckwalter, P.2
-
73
-
-
0036964255
-
The etiological relationship between reading disability and phonological disorder
-
Tunick R, Pennington B (2002) The etiological relationship between reading disability and phonological disorder. Ann Dyslexia 52:75-95
-
(2002)
Ann Dyslexia
, vol.52
, pp. 75-95
-
-
Tunick, R.1
Pennington, B.2
-
74
-
-
13144255748
-
Neural basis of an inherited speech and language disorder
-
Vargha-Khadem F, Watkins KE, Price CJ, Ashburner J, Alcock KJ, Connelly A, Frackowiak RS, Friston KJ, Pembrey ME, Mishkin M, Gadian DG, Passingham RE (1998) Neural basis of an inherited speech and language disorder. Proc Natl Acad Sci USA 95:12695-12700
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 12695-12700
-
-
Vargha-Khadem, F.1
Watkins, K.E.2
Price, C.J.3
Ashburner, J.4
Alcock, K.J.5
Connelly, A.6
Frackowiak, R.S.7
Friston, K.J.8
Pembrey, M.E.9
Mishkin, M.10
Gadian, D.G.11
Passingham, R.E.12
-
75
-
-
0025365999
-
The growth of lexical contraints on spoken word recognition
-
Walley AC, Metsala JL (1990) The growth of lexical contraints on spoken word recognition. Perceptual Psychophysiology 47:267-280
-
(1990)
Perceptual Psychophysiology
, vol.47
, pp. 267-280
-
-
Walley, A.C.1
Metsala, J.L.2
-
78
-
-
0003516538
-
-
The Psychological Corporation, San Antonio, TX
-
- (1992) Wechsler individual achievement test. The Psychological Corporation, San Antonio, TX
-
(1992)
Wechsler Individual Achievement Test
-
-
|