Literature DB >> 8101276

Suggestive linkage of developmental dyslexia to chromosome 1p34-p36.

M Rabin, X L Wen, M Hepburn, H A Lubs, E Feldman, R Duara.   

Abstract

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Year:  1993        PMID: 8101276     DOI: 10.1016/0140-6736(93)91384-x

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  38 in total

1.  Reading disability: evidence for a genetic etiology.

Authors:  J Gayán; R K Olson
Journal:  Eur Child Adolesc Psychiatry       Date:  1999       Impact factor: 4.785

Review 2.  Hyperactivity in children: a focus on genetic research and psychological theories.

Authors:  J Kuntsi; J Stevenson
Journal:  Clin Child Fam Psychol Rev       Date:  2000-03

3.  Evidence for linkage and association with reading disability on 6p21.3-22.

Authors:  D E Kaplan; J Gayán; J Ahn; T-W Won; D Pauls; R K Olson; J C DeFries; F Wood; B F Pennington; G P Page; S D Smith; J R Gruen
Journal:  Am J Hum Genet       Date:  2002-04-10       Impact factor: 11.025

4.  Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.

Authors:  Catherine M Stein; James H Schick; H Gerry Taylor; Lawrence D Shriberg; Christopher Millard; Amy Kundtz-Kluge; Karlie Russo; Nori Minich; Amy Hansen; Lisa A Freebairn; Robert C Elston; Barbara A Lewis; Sudha K Iyengar
Journal:  Am J Hum Genet       Date:  2004-01-20       Impact factor: 11.025

5.  Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses.

Authors:  Karen E Deffenbacher; Judith B Kenyon; Denise M Hoover; Richard K Olson; Bruce F Pennington; John C DeFries; Shelley D Smith
Journal:  Hum Genet       Date:  2004-05-11       Impact factor: 4.132

Review 6.  A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia).

Authors:  S E Fisher; J F Stein; A P Monaco
Journal:  Eur Child Adolesc Psychiatry       Date:  1999       Impact factor: 4.785

Review 7.  Reading and spelling disorders: clinical features and causes.

Authors:  A Warnke
Journal:  Eur Child Adolesc Psychiatry       Date:  1999       Impact factor: 4.785

8.  TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

Authors:  Haiying Meng; Karl Hager; Matthew Held; Grier P Page; Richard K Olson; Bruce F Pennington; John C DeFries; Shelley D Smith; Jeffrey R Gruen
Journal:  Hum Genet       Date:  2005-10-28       Impact factor: 4.132

9.  Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors.

Authors:  Kevin B Rubenstein; Wendy H Raskind; Virginia W Berninger; Mark M Matsushita; Ellen M Wijsman
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2014-05-08       Impact factor: 3.568

10.  Linkage analyses of chromosomal region 18p11-q12 in dyslexia.

Authors:  J Schumacher; I R König; E Plume; P Propping; A Warnke; M Manthey; M Duell; A Kleensang; D Repsilber; M Preis; H Remschmidt; A Ziegler; M M Nöthen; G Schulte-Körne
Journal:  J Neural Transm (Vienna)       Date:  2005-08-03       Impact factor: 3.575

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