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- A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy Journal Article
- A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States Journal Article
- A new locus for dominant drusen and macular degeneration maps to chromosome 6q14 Journal Article
- Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ Journal Article
- Differential genetic etiology of reading component processes as a function of IQ Journal Article
- Etiology of reading difficulties and rapid naming: The Colorado twin study of reading disability Journal Article
- Evidence for linkage and association with reading disability, on 6p21.3-22 Journal Article
- Gene x environment interactions in speech sound disorder predict language and preliteracy outcomes Journal Article
- Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia Journal Article
- Linkage Disequilibrium Mapping of The Chromosome 6q21-22.31 Bipolar I Disorder Susceptibility Locus Journal Article
- Mapping of an autoimmunity susceptibility locus (AIS1) to chromosome 1p31.3-p32.2 Journal Article
- Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit hyperactivity disorder Journal Article
- Quantitative-trait locus for specific language and reading deficits on chromosome 6p Journal Article
- Reading disability and chromosome 6p21.3: Evaluation of MOG as a candidate gene Journal Article
- Reading disability: Evidence for a genetic etiology Journal Article
- Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses Journal Article
- THE HUMAN CONNEXIN GENE FAMILY OF GAP JUNCTION PROTEINS - DISTINCT CHROMOSOMAL LOCATIONS BUT SIMILAR STRUCTURES Journal Article
- The ABCR gene in recessive and dominant Stargardt diseases: A genetic pathway in macular degeneration Journal Article