Familial dyslexia in a large Swedish family: a whole genome linkage scan.
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The genetics of reading disabilities: from phenotypes to candidate genesMutation in CEP63 co-segregating with developmental dyslexia in a Swedish familyMoving closer to a public health model of language and learning disabilities: the role of genetics and the search for etiologiesDCDC2 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.
P2860
Familial dyslexia in a large Swedish family: a whole genome linkage scan.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
@zh-my
2010年学术文章
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2010年學術文章
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name
Familial dyslexia in a large Swedish family: a whole genome linkage scan.
@en
Familial dyslexia in a large Swedish family: a whole genome linkage scan.
@nl
type
label
Familial dyslexia in a large Swedish family: a whole genome linkage scan.
@en
Familial dyslexia in a large Swedish family: a whole genome linkage scan.
@nl
prefLabel
Familial dyslexia in a large Swedish family: a whole genome linkage scan.
@en
Familial dyslexia in a large Swedish family: a whole genome linkage scan.
@nl
P2093
P2860
P1433
P1476
Familial dyslexia in a large Swedish family: a whole genome linkage scan.
@en
P2093
Erland Hjelmquist
Idor Svensson
Jan Wahlström
Lena M Carlsson
Margareta Jernås
P2860
P2888
P356
10.1007/S10519-010-9395-4
P407
P577
2010-09-23T00:00:00Z